Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1318649.RARR44T7G2TFvVi0ChG9s2JWcLtxLJAMgaIh3hVx3KNR0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1318649.RARR44T7G2TFvVi0ChG9s2JWcLtxLJAMgaIh3hVx3KNR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1318649.RARR44T7G2TFvVi0ChG9s2JWcLtxLJAMgaIh3hVx3KNR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1318649.RARR44T7G2TFvVi0ChG9s2JWcLtxLJAMgaIh3hVx3KNR0130_provenance.
- NP1318649.RARR44T7G2TFvVi0ChG9s2JWcLtxLJAMgaIh3hVx3KNR0130_assertion description "[Two new polymorphisms but no mutations of the KIT gene in patients with myelodysplasia at positions corresponding to human FMS and murine W locus mutational hot spots.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1318649.RARR44T7G2TFvVi0ChG9s2JWcLtxLJAMgaIh3hVx3KNR0130_provenance.
- NP1318649.RARR44T7G2TFvVi0ChG9s2JWcLtxLJAMgaIh3hVx3KNR0130_assertion evidence source_evidence_literature NP1318649.RARR44T7G2TFvVi0ChG9s2JWcLtxLJAMgaIh3hVx3KNR0130_provenance.
- NP1318649.RARR44T7G2TFvVi0ChG9s2JWcLtxLJAMgaIh3hVx3KNR0130_assertion SIO_000772 7694008 NP1318649.RARR44T7G2TFvVi0ChG9s2JWcLtxLJAMgaIh3hVx3KNR0130_provenance.
- NP1318649.RARR44T7G2TFvVi0ChG9s2JWcLtxLJAMgaIh3hVx3KNR0130_assertion wasDerivedFrom befree-2016 NP1318649.RARR44T7G2TFvVi0ChG9s2JWcLtxLJAMgaIh3hVx3KNR0130_provenance.
- NP1318649.RARR44T7G2TFvVi0ChG9s2JWcLtxLJAMgaIh3hVx3KNR0130_assertion wasGeneratedBy ECO_0000203 NP1318649.RARR44T7G2TFvVi0ChG9s2JWcLtxLJAMgaIh3hVx3KNR0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1318649.RARR44T7G2TFvVi0ChG9s2JWcLtxLJAMgaIh3hVx3KNR0130_provenance.