@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:NP649277.RAbWJX-ew_f5IIvHe74Fsxdz6GhhbFCQBCUna4zw-aoYg130_head { this: np:hasAssertion dgn-np:NP649277.RAbWJX-ew_f5IIvHe74Fsxdz6GhhbFCQBCUna4zw-aoYg130_assertion; np:hasProvenance dgn-np:NP649277.RAbWJX-ew_f5IIvHe74Fsxdz6GhhbFCQBCUna4zw-aoYg130_provenance; np:hasPublicationInfo dgn-np:NP649277.RAbWJX-ew_f5IIvHe74Fsxdz6GhhbFCQBCUna4zw-aoYg130_publicationInfo; a np:Nanopublication . dgn-np:NP649277.RAbWJX-ew_f5IIvHe74Fsxdz6GhhbFCQBCUna4zw-aoYg130_assertion a np:Assertion . dgn-np:NP649277.RAbWJX-ew_f5IIvHe74Fsxdz6GhhbFCQBCUna4zw-aoYg130_provenance a np:Provenance . dgn-np:NP649277.RAbWJX-ew_f5IIvHe74Fsxdz6GhhbFCQBCUna4zw-aoYg130_publicationInfo a np:PublicationInfo . } dgn-np:NP649277.RAbWJX-ew_f5IIvHe74Fsxdz6GhhbFCQBCUna4zw-aoYg130_assertion { miriam-gene:4436 a ncit:C16612 . lld:C1333990 a ncit:C7057 . dgn-gda:DGN48b569685e48e10e170b1a62e3d42b67 sio:SIO_000628 miriam-gene:4436, lld:C1333990; a sio:SIO_001121 . } dgn-np:NP649277.RAbWJX-ew_f5IIvHe74Fsxdz6GhhbFCQBCUna4zw-aoYg130_provenance { dgn-np:NP649277.RAbWJX-ew_f5IIvHe74Fsxdz6GhhbFCQBCUna4zw-aoYg130_assertion dcterms:description "[This gene belongs to the human DNA mismatch repair system, which is responsible for recognizing and repairing mispaired nucleotides, and mutations in the hMSH2 gene are known to cause hereditary nonpolyposis colorectal cancer (HNPCC).]. 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:18186537; 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:NP649277.RAbWJX-ew_f5IIvHe74Fsxdz6GhhbFCQBCUna4zw-aoYg130_publicationInfo { this: dcterms:created "2016-05-13T12:46:39+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" . }