@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:NP797002.RAoR9DhlyY5WV7oUz0fJl0xxLplqR9_d9KK8i1wv9bQME130_head { this: np:hasAssertion dgn-np:NP797002.RAoR9DhlyY5WV7oUz0fJl0xxLplqR9_d9KK8i1wv9bQME130_assertion; np:hasProvenance dgn-np:NP797002.RAoR9DhlyY5WV7oUz0fJl0xxLplqR9_d9KK8i1wv9bQME130_provenance; np:hasPublicationInfo dgn-np:NP797002.RAoR9DhlyY5WV7oUz0fJl0xxLplqR9_d9KK8i1wv9bQME130_publicationInfo; a np:Nanopublication . dgn-np:NP797002.RAoR9DhlyY5WV7oUz0fJl0xxLplqR9_d9KK8i1wv9bQME130_assertion a np:Assertion . dgn-np:NP797002.RAoR9DhlyY5WV7oUz0fJl0xxLplqR9_d9KK8i1wv9bQME130_provenance a np:Provenance . dgn-np:NP797002.RAoR9DhlyY5WV7oUz0fJl0xxLplqR9_d9KK8i1wv9bQME130_publicationInfo a np:PublicationInfo . } dgn-np:NP797002.RAoR9DhlyY5WV7oUz0fJl0xxLplqR9_d9KK8i1wv9bQME130_assertion { miriam-gene:8493 a ncit:C16612 . lld:C0006142 a ncit:C7057 . dgn-gda:DGN50ddc82d25280d16af0de0f7bcf11968 sio:SIO_000628 miriam-gene:8493, lld:C0006142; a sio:SIO_001121 . } dgn-np:NP797002.RAoR9DhlyY5WV7oUz0fJl0xxLplqR9_d9KK8i1wv9bQME130_provenance { dgn-np:NP797002.RAoR9DhlyY5WV7oUz0fJl0xxLplqR9_d9KK8i1wv9bQME130_assertion dcterms:description "[PPM1D PTV mutations were present in 25 out of 7,781 cases versus 1 out of 5,861 controls (P = 1.12 × 10(-5)), including 18 mutations in 6,912 individuals with breast cancer (P = 2.42 × 10(-4)) and 12 mutations in 1,121 individuals with ovarian cancer (P = 3.10 × 10(-9)).]. 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:23242139; 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:NP797002.RAoR9DhlyY5WV7oUz0fJl0xxLplqR9_d9KK8i1wv9bQME130_publicationInfo { this: dcterms:created "2015-08-25T14:45:42+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" . }