@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:NP521028.RAwVvSQKqhelbBu6EN4JW0k9Cf1J1DaklT6MpxWcQXkYs130_head { this: np:hasAssertion dgn-np:NP521028.RAwVvSQKqhelbBu6EN4JW0k9Cf1J1DaklT6MpxWcQXkYs130_assertion; np:hasProvenance dgn-np:NP521028.RAwVvSQKqhelbBu6EN4JW0k9Cf1J1DaklT6MpxWcQXkYs130_provenance; np:hasPublicationInfo dgn-np:NP521028.RAwVvSQKqhelbBu6EN4JW0k9Cf1J1DaklT6MpxWcQXkYs130_publicationInfo; a np:Nanopublication . dgn-np:NP521028.RAwVvSQKqhelbBu6EN4JW0k9Cf1J1DaklT6MpxWcQXkYs130_assertion a np:Assertion . dgn-np:NP521028.RAwVvSQKqhelbBu6EN4JW0k9Cf1J1DaklT6MpxWcQXkYs130_provenance a np:Provenance . dgn-np:NP521028.RAwVvSQKqhelbBu6EN4JW0k9Cf1J1DaklT6MpxWcQXkYs130_publicationInfo a np:PublicationInfo . } dgn-np:NP521028.RAwVvSQKqhelbBu6EN4JW0k9Cf1J1DaklT6MpxWcQXkYs130_assertion { miriam-gene:4851 a ncit:C16612 . lld:C0596263 a ncit:C7057 . dgn-gda:DGNd43333eff8cbf4f1c34910df22a240de sio:SIO_000628 miriam-gene:4851, lld:C0596263; a sio:SIO_001122 . } dgn-np:NP521028.RAwVvSQKqhelbBu6EN4JW0k9Cf1J1DaklT6MpxWcQXkYs130_provenance { dgn-np:NP521028.RAwVvSQKqhelbBu6EN4JW0k9Cf1J1DaklT6MpxWcQXkYs130_assertion dcterms:description "[Association with other oncogene expression (TAL1, HOXAs, or TLX3/HOX11L2), NOTCH1 activating mutations, and/or CDKN2A/p16/ARF deletion, showed that cyclin D2 dysregulation could contribute to multi-event oncogenesis in various T-ALL groups.]. 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:16270038; 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:NP521028.RAwVvSQKqhelbBu6EN4JW0k9Cf1J1DaklT6MpxWcQXkYs130_publicationInfo { this: dcterms:created "2016-05-13T12:45:41+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" . }