@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:NP418908.RAF04MwTAYXvNxSCbz24eVToAfEVjYcHh3TkOTCGfcWxk130_head { this: np:hasAssertion dgn-np:NP418908.RAF04MwTAYXvNxSCbz24eVToAfEVjYcHh3TkOTCGfcWxk130_assertion; np:hasProvenance dgn-np:NP418908.RAF04MwTAYXvNxSCbz24eVToAfEVjYcHh3TkOTCGfcWxk130_provenance; np:hasPublicationInfo dgn-np:NP418908.RAF04MwTAYXvNxSCbz24eVToAfEVjYcHh3TkOTCGfcWxk130_publicationInfo; a np:Nanopublication . dgn-np:NP418908.RAF04MwTAYXvNxSCbz24eVToAfEVjYcHh3TkOTCGfcWxk130_assertion a np:Assertion . dgn-np:NP418908.RAF04MwTAYXvNxSCbz24eVToAfEVjYcHh3TkOTCGfcWxk130_provenance a np:Provenance . dgn-np:NP418908.RAF04MwTAYXvNxSCbz24eVToAfEVjYcHh3TkOTCGfcWxk130_publicationInfo a np:PublicationInfo . } dgn-np:NP418908.RAF04MwTAYXvNxSCbz24eVToAfEVjYcHh3TkOTCGfcWxk130_assertion { miriam-gene:2623 a ncit:C16612 . lld:C3826066 a ncit:C7057 . dgn-gda:DGNa3072ef4f02a8f967f2656a0e2a40832 sio:SIO_000628 miriam-gene:2623, lld:C3826066; a sio:SIO_001122 . } dgn-np:NP418908.RAF04MwTAYXvNxSCbz24eVToAfEVjYcHh3TkOTCGfcWxk130_provenance { dgn-np:NP418908.RAF04MwTAYXvNxSCbz24eVToAfEVjYcHh3TkOTCGfcWxk130_assertion dcterms:description "[Four years ago it was discovered that nearly all cases of transient myeloproliferative disorder and acute megakaryocytic leukemia in children with Down syndrome acquire mutations in the hematopoietic transcription factor gene GATA1.]. 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:17224656; 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:NP418908.RAF04MwTAYXvNxSCbz24eVToAfEVjYcHh3TkOTCGfcWxk130_publicationInfo { this: dcterms:created "2015-08-25T14:41:43+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" . }