@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:NP620748.RAdcgfwTTUytWoN6EjPQFTNdjTAE6Silf8DMCA-_ZJFt4130_head { this: np:hasAssertion dgn-np:NP620748.RAdcgfwTTUytWoN6EjPQFTNdjTAE6Silf8DMCA-_ZJFt4130_assertion; np:hasProvenance dgn-np:NP620748.RAdcgfwTTUytWoN6EjPQFTNdjTAE6Silf8DMCA-_ZJFt4130_provenance; np:hasPublicationInfo dgn-np:NP620748.RAdcgfwTTUytWoN6EjPQFTNdjTAE6Silf8DMCA-_ZJFt4130_publicationInfo; a np:Nanopublication . dgn-np:NP620748.RAdcgfwTTUytWoN6EjPQFTNdjTAE6Silf8DMCA-_ZJFt4130_assertion a np:Assertion . dgn-np:NP620748.RAdcgfwTTUytWoN6EjPQFTNdjTAE6Silf8DMCA-_ZJFt4130_provenance a np:Provenance . dgn-np:NP620748.RAdcgfwTTUytWoN6EjPQFTNdjTAE6Silf8DMCA-_ZJFt4130_publicationInfo a np:PublicationInfo . } dgn-np:NP620748.RAdcgfwTTUytWoN6EjPQFTNdjTAE6Silf8DMCA-_ZJFt4130_assertion { miriam-gene:4090 a ncit:C16612 . lld:C0026986 a ncit:C7057 . dgn-gda:DGN81c55c4bea2b9db2f8b520be1c901530 sio:SIO_000628 miriam-gene:4090, lld:C0026986; a sio:SIO_001121 . } dgn-np:NP620748.RAdcgfwTTUytWoN6EjPQFTNdjTAE6Silf8DMCA-_ZJFt4130_provenance { dgn-np:NP620748.RAdcgfwTTUytWoN6EjPQFTNdjTAE6Silf8DMCA-_ZJFt4130_assertion dcterms:description "[However, there have been no identified mutations of SMAD5, although the gene localizes to the critical region of loss in chromosome 5q31.1 (chromosome 5, long arm, region 3, band 1, subband 1) in myelodysplasia (MDS) and acute myelogenous leukemia (AML).]. 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:10845932; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP620748.RAdcgfwTTUytWoN6EjPQFTNdjTAE6Silf8DMCA-_ZJFt4130_publicationInfo { this: dcterms:created "2014-10-02T12:38:15+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }