@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:NP569923.RA4rXP2-wwiStEHGveYxgL2bINE1dGtKdM6LEK5BQ30gE130_head { this: np:hasAssertion dgn-np:NP569923.RA4rXP2-wwiStEHGveYxgL2bINE1dGtKdM6LEK5BQ30gE130_assertion; np:hasProvenance dgn-np:NP569923.RA4rXP2-wwiStEHGveYxgL2bINE1dGtKdM6LEK5BQ30gE130_provenance; np:hasPublicationInfo dgn-np:NP569923.RA4rXP2-wwiStEHGveYxgL2bINE1dGtKdM6LEK5BQ30gE130_publicationInfo; a np:Nanopublication . dgn-np:NP569923.RA4rXP2-wwiStEHGveYxgL2bINE1dGtKdM6LEK5BQ30gE130_assertion a np:Assertion . dgn-np:NP569923.RA4rXP2-wwiStEHGveYxgL2bINE1dGtKdM6LEK5BQ30gE130_provenance a np:Provenance . dgn-np:NP569923.RA4rXP2-wwiStEHGveYxgL2bINE1dGtKdM6LEK5BQ30gE130_publicationInfo a np:PublicationInfo . } dgn-np:NP569923.RA4rXP2-wwiStEHGveYxgL2bINE1dGtKdM6LEK5BQ30gE130_assertion { miriam-gene:4436 a ncit:C16612 . lld:C0029925 a ncit:C7057 . dgn-gda:DGNdd0d753a4551e4f5af1d28d26edad5d8 sio:SIO_000628 miriam-gene:4436, lld:C0029925; a sio:SIO_001121 . } dgn-np:NP569923.RA4rXP2-wwiStEHGveYxgL2bINE1dGtKdM6LEK5BQ30gE130_provenance { dgn-np:NP569923.RA4rXP2-wwiStEHGveYxgL2bINE1dGtKdM6LEK5BQ30gE130_assertion dcterms:description "[The incidence of germline MMR gene mutations in ovarian cancer is only 2% but other mechanisms of gene inactivation mean that loss of expression of one of the seven main genes (MSH2, MSH3, MSH6, MLH1, MLH3, PMS1 and PMS2) occurs in up to 29% of cases.]. 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:24333356; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP569923.RA4rXP2-wwiStEHGveYxgL2bINE1dGtKdM6LEK5BQ30gE130_publicationInfo { this: dcterms:created "2015-08-25T14:43:19+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }