Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP580204.RAB0k_39FCGrlxStG74T3GWrgVRB_rgm1gzIkuqs6FMWY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP580204.RAB0k_39FCGrlxStG74T3GWrgVRB_rgm1gzIkuqs6FMWY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP580204.RAB0k_39FCGrlxStG74T3GWrgVRB_rgm1gzIkuqs6FMWY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP580204.RAB0k_39FCGrlxStG74T3GWrgVRB_rgm1gzIkuqs6FMWY130_provenance.
- NP580204.RAB0k_39FCGrlxStG74T3GWrgVRB_rgm1gzIkuqs6FMWY130_assertion description "[This is the first report ever described for patients with CLPD and MDS and/or MPD shown to arise from distinct chromosomal abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580204.RAB0k_39FCGrlxStG74T3GWrgVRB_rgm1gzIkuqs6FMWY130_provenance.
- NP580204.RAB0k_39FCGrlxStG74T3GWrgVRB_rgm1gzIkuqs6FMWY130_assertion evidence source_evidence_literature NP580204.RAB0k_39FCGrlxStG74T3GWrgVRB_rgm1gzIkuqs6FMWY130_provenance.
- NP580204.RAB0k_39FCGrlxStG74T3GWrgVRB_rgm1gzIkuqs6FMWY130_assertion SIO_000772 11378546 NP580204.RAB0k_39FCGrlxStG74T3GWrgVRB_rgm1gzIkuqs6FMWY130_provenance.
- NP580204.RAB0k_39FCGrlxStG74T3GWrgVRB_rgm1gzIkuqs6FMWY130_assertion wasDerivedFrom befree-20150227 NP580204.RAB0k_39FCGrlxStG74T3GWrgVRB_rgm1gzIkuqs6FMWY130_provenance.
- NP580204.RAB0k_39FCGrlxStG74T3GWrgVRB_rgm1gzIkuqs6FMWY130_assertion wasGeneratedBy ECO_0000203 NP580204.RAB0k_39FCGrlxStG74T3GWrgVRB_rgm1gzIkuqs6FMWY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP580204.RAB0k_39FCGrlxStG74T3GWrgVRB_rgm1gzIkuqs6FMWY130_provenance.