@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:NP463529.RAGQFBLzyk-YEGcI1Wj9oC5rRfvGQ-9Qe9jhOElmYi7uo130_head { this: np:hasAssertion dgn-np:NP463529.RAGQFBLzyk-YEGcI1Wj9oC5rRfvGQ-9Qe9jhOElmYi7uo130_assertion; np:hasProvenance dgn-np:NP463529.RAGQFBLzyk-YEGcI1Wj9oC5rRfvGQ-9Qe9jhOElmYi7uo130_provenance; np:hasPublicationInfo dgn-np:NP463529.RAGQFBLzyk-YEGcI1Wj9oC5rRfvGQ-9Qe9jhOElmYi7uo130_publicationInfo; a np:Nanopublication . dgn-np:NP463529.RAGQFBLzyk-YEGcI1Wj9oC5rRfvGQ-9Qe9jhOElmYi7uo130_assertion a np:Assertion . dgn-np:NP463529.RAGQFBLzyk-YEGcI1Wj9oC5rRfvGQ-9Qe9jhOElmYi7uo130_provenance a np:Provenance . dgn-np:NP463529.RAGQFBLzyk-YEGcI1Wj9oC5rRfvGQ-9Qe9jhOElmYi7uo130_publicationInfo a np:PublicationInfo . } dgn-np:NP463529.RAGQFBLzyk-YEGcI1Wj9oC5rRfvGQ-9Qe9jhOElmYi7uo130_assertion { miriam-gene:4851 a ncit:C16612 . lld:C0032064 a ncit:C7057 . dgn-gda:DGN63f798fd21eb43d0bae6acd95a41d4d8 sio:SIO_000628 miriam-gene:4851, lld:C0032064; a sio:SIO_001121 . } dgn-np:NP463529.RAGQFBLzyk-YEGcI1Wj9oC5rRfvGQ-9Qe9jhOElmYi7uo130_provenance { dgn-np:NP463529.RAGQFBLzyk-YEGcI1Wj9oC5rRfvGQ-9Qe9jhOElmYi7uo130_assertion dcterms:description "[Here, we report that more than 50% of human T-ALLs, including tumors from all major molecular oncogenic subtypes, have activating mutations that involve the extracellular heterodimerization domain and/or the C-terminal PEST domain of NOTCH1.]. 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:15472075; 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:NP463529.RAGQFBLzyk-YEGcI1Wj9oC5rRfvGQ-9Qe9jhOElmYi7uo130_publicationInfo { this: dcterms:created "2016-05-13T12:45:15+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" . }