@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:NP869556.RASMM08d40U5e2KFqn6nsgxPuNbXRylidWWo3jM2C4tUU130_head { this: np:hasAssertion dgn-np:NP869556.RASMM08d40U5e2KFqn6nsgxPuNbXRylidWWo3jM2C4tUU130_assertion; np:hasProvenance dgn-np:NP869556.RASMM08d40U5e2KFqn6nsgxPuNbXRylidWWo3jM2C4tUU130_provenance; np:hasPublicationInfo dgn-np:NP869556.RASMM08d40U5e2KFqn6nsgxPuNbXRylidWWo3jM2C4tUU130_publicationInfo; a np:Nanopublication . dgn-np:NP869556.RASMM08d40U5e2KFqn6nsgxPuNbXRylidWWo3jM2C4tUU130_assertion a np:Assertion . dgn-np:NP869556.RASMM08d40U5e2KFqn6nsgxPuNbXRylidWWo3jM2C4tUU130_provenance a np:Provenance . dgn-np:NP869556.RASMM08d40U5e2KFqn6nsgxPuNbXRylidWWo3jM2C4tUU130_publicationInfo a np:PublicationInfo . } dgn-np:NP869556.RASMM08d40U5e2KFqn6nsgxPuNbXRylidWWo3jM2C4tUU130_assertion { miriam-gene:4436 a ncit:C16612 . lld:C0009402 a ncit:C7057 . dgn-gda:DGN951af0ae1b21e2359fd22a1e9b5f84f4 sio:SIO_000628 miriam-gene:4436, lld:C0009402; a sio:SIO_001121 . } dgn-np:NP869556.RASMM08d40U5e2KFqn6nsgxPuNbXRylidWWo3jM2C4tUU130_provenance { dgn-np:NP869556.RASMM08d40U5e2KFqn6nsgxPuNbXRylidWWo3jM2C4tUU130_assertion dcterms:description "[A cohort of 206 consecutively-collected patients with colorectal carcinoma (CRC) were screened for germline mutations in the principal DNA mismatch repair (MMR) genes, MLH1 and MSH2, and in the Fanconi anemia (FA) genes involved in homologous recombination DNA repair.]. 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:21286667; 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:NP869556.RASMM08d40U5e2KFqn6nsgxPuNbXRylidWWo3jM2C4tUU130_publicationInfo { this: dcterms:created "2016-05-13T12:48:18+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" . }