@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:NP969773.RAW6ZIm3MkJW5DT1pdafqYlvbudbmqx4ORs0JcVhZh7PU130_head { this: np:hasAssertion dgn-np:NP969773.RAW6ZIm3MkJW5DT1pdafqYlvbudbmqx4ORs0JcVhZh7PU130_assertion; np:hasProvenance dgn-np:NP969773.RAW6ZIm3MkJW5DT1pdafqYlvbudbmqx4ORs0JcVhZh7PU130_provenance; np:hasPublicationInfo dgn-np:NP969773.RAW6ZIm3MkJW5DT1pdafqYlvbudbmqx4ORs0JcVhZh7PU130_publicationInfo; a np:Nanopublication . dgn-np:NP969773.RAW6ZIm3MkJW5DT1pdafqYlvbudbmqx4ORs0JcVhZh7PU130_assertion a np:Assertion . dgn-np:NP969773.RAW6ZIm3MkJW5DT1pdafqYlvbudbmqx4ORs0JcVhZh7PU130_provenance a np:Provenance . dgn-np:NP969773.RAW6ZIm3MkJW5DT1pdafqYlvbudbmqx4ORs0JcVhZh7PU130_publicationInfo a np:PublicationInfo . } dgn-np:NP969773.RAW6ZIm3MkJW5DT1pdafqYlvbudbmqx4ORs0JcVhZh7PU130_assertion { miriam-gene:4524 a ncit:C16612 . lld:C0023467 a ncit:C7057 . dgn-gda:DGNa9a159ad031febf5a3d8287f82260cea sio:SIO_000628 miriam-gene:4524, lld:C0023467; a sio:SIO_001122 . } dgn-np:NP969773.RAW6ZIm3MkJW5DT1pdafqYlvbudbmqx4ORs0JcVhZh7PU130_provenance { dgn-np:NP969773.RAW6ZIm3MkJW5DT1pdafqYlvbudbmqx4ORs0JcVhZh7PU130_assertion dcterms:description "[The aim of this case-control study was to evaluate the association of the C677T MTHFR gene polymorphism with acute myeloid leukaemia (AML), acute lymphoblastic leukaemia (ALL), chronic myeloid leukaemia (CML) and chronic lymphocytic leukaemia (CLL).]. 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:22441130; 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:NP969773.RAW6ZIm3MkJW5DT1pdafqYlvbudbmqx4ORs0JcVhZh7PU130_publicationInfo { this: dcterms:created "2016-05-13T12:49:04+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" . }