@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:NP1362989.RAu4golZ3b8uHzXt3xXOl9cLdYK8v8Gk18CKNv1-1_xN4130_head { this: np:hasAssertion dgn-np:NP1362989.RAu4golZ3b8uHzXt3xXOl9cLdYK8v8Gk18CKNv1-1_xN4130_assertion; np:hasProvenance dgn-np:NP1362989.RAu4golZ3b8uHzXt3xXOl9cLdYK8v8Gk18CKNv1-1_xN4130_provenance; np:hasPublicationInfo dgn-np:NP1362989.RAu4golZ3b8uHzXt3xXOl9cLdYK8v8Gk18CKNv1-1_xN4130_publicationInfo; a np:Nanopublication . dgn-np:NP1362989.RAu4golZ3b8uHzXt3xXOl9cLdYK8v8Gk18CKNv1-1_xN4130_assertion a np:Assertion . dgn-np:NP1362989.RAu4golZ3b8uHzXt3xXOl9cLdYK8v8Gk18CKNv1-1_xN4130_provenance a np:Provenance . dgn-np:NP1362989.RAu4golZ3b8uHzXt3xXOl9cLdYK8v8Gk18CKNv1-1_xN4130_publicationInfo a np:PublicationInfo . } dgn-np:NP1362989.RAu4golZ3b8uHzXt3xXOl9cLdYK8v8Gk18CKNv1-1_xN4130_assertion { miriam-gene:4292 a ncit:C16612 . lld:C1527249 a ncit:C7057 . dgn-gda:DGN330766fee7519d07a8adfb1eb0cb590f sio:SIO_000628 miriam-gene:4292, lld:C1527249; a sio:SIO_001121 . } dgn-np:NP1362989.RAu4golZ3b8uHzXt3xXOl9cLdYK8v8Gk18CKNv1-1_xN4130_provenance { dgn-np:NP1362989.RAu4golZ3b8uHzXt3xXOl9cLdYK8v8Gk18CKNv1-1_xN4130_assertion dcterms:description "[Taken together with previous studies which focused on colorectal cancers from HNPCC families, the data suggest that allele loss at hMLH1, but not at hMSH2, contributes to defective mismatch repair in inherited and sporadic colorectal cancer.]. 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:8932328; 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:NP1362989.RAu4golZ3b8uHzXt3xXOl9cLdYK8v8Gk18CKNv1-1_xN4130_publicationInfo { this: dcterms:created "2016-05-13T12:52:04+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" . }