@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:NP372565.RAi8Q0EahuKSQIfAB0SmVX7mT9c434Ww9XkR78cR8h8dk130_head { this: np:hasAssertion dgn-np:NP372565.RAi8Q0EahuKSQIfAB0SmVX7mT9c434Ww9XkR78cR8h8dk130_assertion; np:hasProvenance dgn-np:NP372565.RAi8Q0EahuKSQIfAB0SmVX7mT9c434Ww9XkR78cR8h8dk130_provenance; np:hasPublicationInfo dgn-np:NP372565.RAi8Q0EahuKSQIfAB0SmVX7mT9c434Ww9XkR78cR8h8dk130_publicationInfo; a np:Nanopublication . dgn-np:NP372565.RAi8Q0EahuKSQIfAB0SmVX7mT9c434Ww9XkR78cR8h8dk130_assertion a np:Assertion . dgn-np:NP372565.RAi8Q0EahuKSQIfAB0SmVX7mT9c434Ww9XkR78cR8h8dk130_provenance a np:Provenance . dgn-np:NP372565.RAi8Q0EahuKSQIfAB0SmVX7mT9c434Ww9XkR78cR8h8dk130_publicationInfo a np:PublicationInfo . } dgn-np:NP372565.RAi8Q0EahuKSQIfAB0SmVX7mT9c434Ww9XkR78cR8h8dk130_assertion { miriam-gene:1029 a ncit:C16612 . lld:C1140680 a ncit:C7057 . dgn-gda:DGN02ec51b874c35596907db283b5fc3feb sio:SIO_000628 miriam-gene:1029, lld:C1140680; a sio:SIO_001121 . } dgn-np:NP372565.RAi8Q0EahuKSQIfAB0SmVX7mT9c434Ww9XkR78cR8h8dk130_provenance { dgn-np:NP372565.RAi8Q0EahuKSQIfAB0SmVX7mT9c434Ww9XkR78cR8h8dk130_assertion dcterms:description "[Several reports have implicated alterations of the hMLH1 and p16(ink4a) (p16) genes, in particular hypermethylation of the promoter region, and of the PTEN gene, principally genetic mutations, in endometrial and ovarian cancers and have indicated that these alterations are already present in precancer conditions.]. 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:12402310; 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:NP372565.RAi8Q0EahuKSQIfAB0SmVX7mT9c434Ww9XkR78cR8h8dk130_publicationInfo { this: dcterms:created "2016-05-13T12:44:34+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" . }