0) { for (i = 0; i < cbs.length; i++) { cbs[i](); } } }); return { then: function(cb) { cb && (loaded ? cb() : (cbs.push(cb))); } }; })(); })(); (function() { window.throttle = function(func, wait) { var args, result, thisArg, timeoutId, lastCalled = 0; function trailingCall() { lastCalled = new Date; timeoutId = null; result = func.apply(thisArg, args); } return function() { var now = new Date, remaining = wait - (now - lastCalled); args = arguments; thisArg = this; if (remaining <= 0) { clearTimeout(timeoutId); timeoutId = null; lastCalled = now; result = func.apply(thisArg, args); } else if (!timeoutId) { timeoutId = setTimeout(trailingCall, remaining); } return result; }; }; })(); (function() { var Set = (function() { var add = function(item) { var i, data = this._data; for (i = 0; i < data.length; i++) { if (data[i] === item) { return; } } this.size ++; data.push(item); return data; }; var Set = function(data) { this.size = 0; this._data = []; var i; if (data.length > 0) { for (i = 0; i < data.length; i++) { add.call(this, data[i]); } } }; Set.prototype.add = add; Set.prototype.get = function(index) { return this._data[index]; }; Set.prototype.has = function(item) { var i, data = this._data; for (i = 0; i < data.length; i++) { if (this.get(i) === item) { return true; } } return false; }; Set.prototype.is = function(map) { if (map._data.length !== this._data.length) { return false; } var i, j, flag, tData = this._data, mData = map._data; for (i = 0; i < tData.length; i++) { for (flag = false, j = 0; j < mData.length; j++) { if (tData[i] === mData[j]) { flag = true; break; } } if (!flag) { return false; } } return true; }; Set.prototype.values = function() { return this._data; }; return Set; })(); window.Lazyload = (function(doc) { var queue = {js: [], css: []}, sources = {js: {}, css: {}}, context = this; var createNode = function(name, attrs) { var node = doc.createElement(name), attr; for (attr in attrs) { if (attrs.hasOwnProperty(attr)) { node.setAttribute(attr, attrs[attr]); } } return node; }; var end = function(type, url) { var s, q, qi, cbs, i, j, cur, val, flag; if (type === 'js' || type ==='css') { s = sources[type], q = queue[type]; s[url] = true; for (i = 0; i < q.length; i++) { cur = q[i]; if (cur.urls.has(url)) { qi = cur, val = qi.urls.values(); qi && (cbs = qi.callbacks); for (flag = true, j = 0; j < val.length; j++) { cur = val[j]; if (!s[cur]) { flag = false; } } if (flag && cbs && cbs.length > 0) { for (j = 0; j < cbs.length; j++) { cbs[j].call(context); } qi.load = true; } } } } }; var load = function(type, urls, callback) { var s, q, qi, node, i, cur, _urls = typeof urls === 'string' ? new Set([urls]) : new Set(urls), val, url; if (type === 'js' || type ==='css') { s = sources[type], q = queue[type]; for (i = 0; i < q.length; i++) { cur = q[i]; if (_urls.is(cur.urls)) { qi = cur; break; } } val = _urls.values(); if (qi) { callback && (qi.load || qi.callbacks.push(callback)); callback && (qi.load && callback()); } else { q.push({ urls: _urls, callbacks: callback ? [callback] : [], load: false }); for (i = 0; i < val.length; i++) { node = null, url = val[i]; if (s[url] === undefined) { (type === 'js' ) && (node = createNode('script', { src: url })); (type === 'css') && (node = createNode('link', { rel: 'stylesheet', href: url })); if (node) { node.onload = (function(type, url) { return function() { end(type, url); }; })(type, url); (doc.head || doc.body).appendChild(node); s[url] = false; } } } } } }; return { js: function(url, callback) { load('js', url, callback); }, css: function(url, callback) { load('css', url, callback); } }; })(this.document); })();

Pipeline to Extract the Names of Drugs & Chemicals

Description

This pretrained pipeline is built on the top of ner_chemd_clinical model.

Predicted Entities

Copy S3 URI

How to use

from sparknlp.pretrained import PretrainedPipeline

pipeline = PretrainedPipeline("ner_chemd_clinical_pipeline", "en", "clinical/models")

text = '''Isolation, Structure Elucidation, and Iron-Binding Properties of Lystabactins, Siderophores Isolated from a Marine Pseudoalteromonas sp. The marine bacterium Pseudoalteromonas sp. S2B, isolated from the Gulf of Mexico after the Deepwater Horizon oil spill, was found to produce lystabactins A, B, and C (1-3), three new siderophores. The structures were elucidated through mass spectrometry, amino acid analysis, and NMR. The lystabactins are composed of serine (Ser), asparagine (Asn), two formylated/hydroxylated ornithines (FOHOrn), dihydroxy benzoic acid (Dhb), and a very unusual nonproteinogenic amino acid, 4,8-diamino-3-hydroxyoctanoic acid (LySta). The iron-binding properties of the compounds were investigated through a spectrophotometric competition.'''

result = pipeline.fullAnnotate(text)
import com.johnsnowlabs.nlp.pretrained.PretrainedPipeline

val pipeline = new PretrainedPipeline("ner_chemd_clinical_pipeline", "en", "clinical/models")

val text = "Isolation, Structure Elucidation, and Iron-Binding Properties of Lystabactins, Siderophores Isolated from a Marine Pseudoalteromonas sp. The marine bacterium Pseudoalteromonas sp. S2B, isolated from the Gulf of Mexico after the Deepwater Horizon oil spill, was found to produce lystabactins A, B, and C (1-3), three new siderophores. The structures were elucidated through mass spectrometry, amino acid analysis, and NMR. The lystabactins are composed of serine (Ser), asparagine (Asn), two formylated/hydroxylated ornithines (FOHOrn), dihydroxy benzoic acid (Dhb), and a very unusual nonproteinogenic amino acid, 4,8-diamino-3-hydroxyoctanoic acid (LySta). The iron-binding properties of the compounds were investigated through a spectrophotometric competition."

val result = pipeline.fullAnnotate(text)
from sparknlp.pretrained import PretrainedPipeline

pipeline = PretrainedPipeline("ner_chemd_clinical_pipeline", "en", "clinical/models")

text = '''Isolation, Structure Elucidation, and Iron-Binding Properties of Lystabactins, Siderophores Isolated from a Marine Pseudoalteromonas sp. The marine bacterium Pseudoalteromonas sp. S2B, isolated from the Gulf of Mexico after the Deepwater Horizon oil spill, was found to produce lystabactins A, B, and C (1-3), three new siderophores. The structures were elucidated through mass spectrometry, amino acid analysis, and NMR. The lystabactins are composed of serine (Ser), asparagine (Asn), two formylated/hydroxylated ornithines (FOHOrn), dihydroxy benzoic acid (Dhb), and a very unusual nonproteinogenic amino acid, 4,8-diamino-3-hydroxyoctanoic acid (LySta). The iron-binding properties of the compounds were investigated through a spectrophotometric competition.'''

result = pipeline.fullAnnotate(text)

Results

|    | ner_chunks                         |   begin |   end | ner_label    |   confidence |
|---:|:-----------------------------------|--------:|------:|:-------------|-------------:|
|  0 | Lystabactins                       |      65 |    76 | FAMILY       |     0.9841   |
|  1 | lystabactins A, B, and C           |     278 |   301 | MULTIPLE     |     0.813429 |
|  2 | amino acid                         |     392 |   401 | FAMILY       |     0.74585  |
|  3 | lystabactins                       |     426 |   437 | FAMILY       |     0.8007   |
|  4 | serine                             |     455 |   460 | TRIVIAL      |     0.9924   |
|  5 | Ser                                |     463 |   465 | FORMULA      |     0.9999   |
|  6 | asparagine                         |     469 |   478 | TRIVIAL      |     0.9795   |
|  7 | Asn                                |     481 |   483 | FORMULA      |     0.9999   |
|  8 | formylated/hydroxylated ornithines |     491 |   524 | FAMILY       |     0.50085  |
|  9 | FOHOrn                             |     527 |   532 | FORMULA      |     0.509    |
| 10 | dihydroxy benzoic acid             |     536 |   557 | SYSTEMATIC   |     0.6346   |
| 11 | amino acid                         |     602 |   611 | FAMILY       |     0.4204   |
| 12 | 4,8-diamino-3-hydroxyoctanoic acid |     614 |   647 | SYSTEMATIC   |     0.9124   |
| 13 | LySta                              |     650 |   654 | ABBREVIATION |     0.9193   |

Model Information

Model Name: ner_chemd_clinical_pipeline
Type: pipeline
Compatibility: Healthcare NLP 4.4.4+
License: Licensed
Edition: Official
Language: en
Size: 1.7 GB

Included Models

  • DocumentAssembler
  • SentenceDetectorDLModel
  • TokenizerModel
  • WordEmbeddingsModel
  • MedicalNerModel
  • NerConverterInternalModel