@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:NP929155.RAprIbnXi0rm7QffD3utQLxsw74a5MkyfA3g_vm4b2AGk130_head { this: np:hasAssertion dgn-np:NP929155.RAprIbnXi0rm7QffD3utQLxsw74a5MkyfA3g_vm4b2AGk130_assertion; np:hasProvenance dgn-np:NP929155.RAprIbnXi0rm7QffD3utQLxsw74a5MkyfA3g_vm4b2AGk130_provenance; np:hasPublicationInfo dgn-np:NP929155.RAprIbnXi0rm7QffD3utQLxsw74a5MkyfA3g_vm4b2AGk130_publicationInfo; a np:Nanopublication . dgn-np:NP929155.RAprIbnXi0rm7QffD3utQLxsw74a5MkyfA3g_vm4b2AGk130_assertion a np:Assertion . dgn-np:NP929155.RAprIbnXi0rm7QffD3utQLxsw74a5MkyfA3g_vm4b2AGk130_provenance a np:Provenance . dgn-np:NP929155.RAprIbnXi0rm7QffD3utQLxsw74a5MkyfA3g_vm4b2AGk130_publicationInfo a np:PublicationInfo . } dgn-np:NP929155.RAprIbnXi0rm7QffD3utQLxsw74a5MkyfA3g_vm4b2AGk130_assertion { miriam-gene:1788 a ncit:C16612 . lld:C0023467 a ncit:C7057 . dgn-gda:DGN3e72a846e77a821c2cbfc863d9bcecc5 sio:SIO_000628 miriam-gene:1788, lld:C0023467; a sio:SIO_001121 . } dgn-np:NP929155.RAprIbnXi0rm7QffD3utQLxsw74a5MkyfA3g_vm4b2AGk130_provenance { dgn-np:NP929155.RAprIbnXi0rm7QffD3utQLxsw74a5MkyfA3g_vm4b2AGk130_assertion dcterms:description "[Here we describe the consequences of single amino acid mutations, including those implicated in the development of acute myeloid leukemia (AML) and myelodysplastic syndromes, at the DNMT3A·DNMT3A homotetramer and DNMT3A·DNMT3L heterotetramer interfaces.]. 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:21979949; 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:NP929155.RAprIbnXi0rm7QffD3utQLxsw74a5MkyfA3g_vm4b2AGk130_publicationInfo { this: dcterms:created "2016-05-13T12:48:46+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" . }