http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU#head http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU#assertion http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU#provenance http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU#assertion http://rdf.disgenet.org/resource/gda/DGNa411462c2192090178d743bee0e0771c http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/5395 http://rdf.disgenet.org/resource/gda/DGNa411462c2192090178d743bee0e0771c http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C1333990 http://rdf.disgenet.org/resource/gda/DGNa411462c2192090178d743bee0e0771c http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001123 http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU#provenance http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU#assertion http://purl.org/dc/terms/description [The high frequency of MLH1 germline mutations identified in our study has important implications for testing strategies in patients suspected of having Lynch syndrome and indicates that patients with tumors demonstrating isolated loss of PMS2 expression without a germline PMS2 mutation must have MLH1 mutation analysis performed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/25871621 http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://purl.org/dc/terms/created 2017-10-17T13:15:30+02:00 http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP835346.RA8Qxy2h2BTfOqsgXARxCFuS32gsPneFSePA-fbcbWvzU http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0