Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583502.RAd_rT1RyUOWz1pfnEU6EkymZVbWxO9XMykbT9XmcXseo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583502.RAd_rT1RyUOWz1pfnEU6EkymZVbWxO9XMykbT9XmcXseo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583502.RAd_rT1RyUOWz1pfnEU6EkymZVbWxO9XMykbT9XmcXseo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583502.RAd_rT1RyUOWz1pfnEU6EkymZVbWxO9XMykbT9XmcXseo130_provenance.
- NP583502.RAd_rT1RyUOWz1pfnEU6EkymZVbWxO9XMykbT9XmcXseo130_assertion description "[Thus, our results suggest that mutations in MYH9 result in three megakaryocyte/platelet/leukocyte syndromes and are important in the pathogenesis of sensorineural deafness, cataracts and nephritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583502.RAd_rT1RyUOWz1pfnEU6EkymZVbWxO9XMykbT9XmcXseo130_provenance.
- NP583502.RAd_rT1RyUOWz1pfnEU6EkymZVbWxO9XMykbT9XmcXseo130_assertion evidence source_evidence_literature NP583502.RAd_rT1RyUOWz1pfnEU6EkymZVbWxO9XMykbT9XmcXseo130_provenance.
- NP583502.RAd_rT1RyUOWz1pfnEU6EkymZVbWxO9XMykbT9XmcXseo130_assertion SIO_000772 10973259 NP583502.RAd_rT1RyUOWz1pfnEU6EkymZVbWxO9XMykbT9XmcXseo130_provenance.
- NP583502.RAd_rT1RyUOWz1pfnEU6EkymZVbWxO9XMykbT9XmcXseo130_assertion wasDerivedFrom befree-20150227 NP583502.RAd_rT1RyUOWz1pfnEU6EkymZVbWxO9XMykbT9XmcXseo130_provenance.
- NP583502.RAd_rT1RyUOWz1pfnEU6EkymZVbWxO9XMykbT9XmcXseo130_assertion wasGeneratedBy ECO_0000203 NP583502.RAd_rT1RyUOWz1pfnEU6EkymZVbWxO9XMykbT9XmcXseo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583502.RAd_rT1RyUOWz1pfnEU6EkymZVbWxO9XMykbT9XmcXseo130_provenance.