Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP726596.RAKJk8ibNErjtVg4k2GKhquVDUQIEkwdQP55sAAj6UMRk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP726596.RAKJk8ibNErjtVg4k2GKhquVDUQIEkwdQP55sAAj6UMRk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP726596.RAKJk8ibNErjtVg4k2GKhquVDUQIEkwdQP55sAAj6UMRk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP726596.RAKJk8ibNErjtVg4k2GKhquVDUQIEkwdQP55sAAj6UMRk130_provenance.
- NP726596.RAKJk8ibNErjtVg4k2GKhquVDUQIEkwdQP55sAAj6UMRk130_assertion description "[Recessive mutations in CUBN or AMN cause Imerslund-Gr�sbeck Syndrome (IGS), while recessive mutations in GIF cause Intrinsic Factor Deficiency (IFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP726596.RAKJk8ibNErjtVg4k2GKhquVDUQIEkwdQP55sAAj6UMRk130_provenance.
- NP726596.RAKJk8ibNErjtVg4k2GKhquVDUQIEkwdQP55sAAj6UMRk130_assertion evidence source_evidence_literature NP726596.RAKJk8ibNErjtVg4k2GKhquVDUQIEkwdQP55sAAj6UMRk130_provenance.
- NP726596.RAKJk8ibNErjtVg4k2GKhquVDUQIEkwdQP55sAAj6UMRk130_assertion SIO_000772 22929189 NP726596.RAKJk8ibNErjtVg4k2GKhquVDUQIEkwdQP55sAAj6UMRk130_provenance.
- NP726596.RAKJk8ibNErjtVg4k2GKhquVDUQIEkwdQP55sAAj6UMRk130_assertion wasDerivedFrom befree-20140225 NP726596.RAKJk8ibNErjtVg4k2GKhquVDUQIEkwdQP55sAAj6UMRk130_provenance.
- NP726596.RAKJk8ibNErjtVg4k2GKhquVDUQIEkwdQP55sAAj6UMRk130_assertion wasGeneratedBy ECO_0000203 NP726596.RAKJk8ibNErjtVg4k2GKhquVDUQIEkwdQP55sAAj6UMRk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP726596.RAKJk8ibNErjtVg4k2GKhquVDUQIEkwdQP55sAAj6UMRk130_provenance.