@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1366020.RAoeUDkiBptNCse9ngxnVqcUQCQGB8AVDSInDH1SiZpYQ130_head { this: np:hasAssertion dgn-np:NP1366020.RAoeUDkiBptNCse9ngxnVqcUQCQGB8AVDSInDH1SiZpYQ130_assertion; np:hasProvenance dgn-np:NP1366020.RAoeUDkiBptNCse9ngxnVqcUQCQGB8AVDSInDH1SiZpYQ130_provenance; np:hasPublicationInfo dgn-np:NP1366020.RAoeUDkiBptNCse9ngxnVqcUQCQGB8AVDSInDH1SiZpYQ130_publicationInfo; a np:Nanopublication . dgn-np:NP1366020.RAoeUDkiBptNCse9ngxnVqcUQCQGB8AVDSInDH1SiZpYQ130_assertion a np:Assertion . dgn-np:NP1366020.RAoeUDkiBptNCse9ngxnVqcUQCQGB8AVDSInDH1SiZpYQ130_provenance a np:Provenance . dgn-np:NP1366020.RAoeUDkiBptNCse9ngxnVqcUQCQGB8AVDSInDH1SiZpYQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP1366020.RAoeUDkiBptNCse9ngxnVqcUQCQGB8AVDSInDH1SiZpYQ130_assertion { miriam-gene:4292 a ncit:C16612 . lld:C1527249 a ncit:C7057 . dgn-gda:DGN1efab6a121fe2d87871bcc6fe4cd48bb sio:SIO_000628 miriam-gene:4292, lld:C1527249; a sio:SIO_001121 . } dgn-np:NP1366020.RAoeUDkiBptNCse9ngxnVqcUQCQGB8AVDSInDH1SiZpYQ130_provenance { dgn-np:NP1366020.RAoeUDkiBptNCse9ngxnVqcUQCQGB8AVDSInDH1SiZpYQ130_assertion dcterms:description "[These findings suggest that most cancers in patients diagnosed at 45 years of age or less and familial aggregations of colorectal cancer which do not fulfil HNPCC diagnostic criteria do not have germline mutations in MSH2 and MLH1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:9004127; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP1366020.RAoeUDkiBptNCse9ngxnVqcUQCQGB8AVDSInDH1SiZpYQ130_publicationInfo { this: dcterms:created "2016-05-13T12:52:05+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }