Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1008709.RA7H6G-HGmz8TwD85KX1NHz1VxOENvocOp7zIQqQ0bMe8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1008709.RA7H6G-HGmz8TwD85KX1NHz1VxOENvocOp7zIQqQ0bMe8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1008709.RA7H6G-HGmz8TwD85KX1NHz1VxOENvocOp7zIQqQ0bMe8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1008709.RA7H6G-HGmz8TwD85KX1NHz1VxOENvocOp7zIQqQ0bMe8130_provenance.
- NP1008709.RA7H6G-HGmz8TwD85KX1NHz1VxOENvocOp7zIQqQ0bMe8130_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." NP1008709.RA7H6G-HGmz8TwD85KX1NHz1VxOENvocOp7zIQqQ0bMe8130_provenance.
- NP1008709.RA7H6G-HGmz8TwD85KX1NHz1VxOENvocOp7zIQqQ0bMe8130_assertion evidence source_evidence_literature NP1008709.RA7H6G-HGmz8TwD85KX1NHz1VxOENvocOp7zIQqQ0bMe8130_provenance.
- NP1008709.RA7H6G-HGmz8TwD85KX1NHz1VxOENvocOp7zIQqQ0bMe8130_assertion SIO_000772 22929189 NP1008709.RA7H6G-HGmz8TwD85KX1NHz1VxOENvocOp7zIQqQ0bMe8130_provenance.
- NP1008709.RA7H6G-HGmz8TwD85KX1NHz1VxOENvocOp7zIQqQ0bMe8130_assertion wasDerivedFrom befree-2016 NP1008709.RA7H6G-HGmz8TwD85KX1NHz1VxOENvocOp7zIQqQ0bMe8130_provenance.
- NP1008709.RA7H6G-HGmz8TwD85KX1NHz1VxOENvocOp7zIQqQ0bMe8130_assertion wasGeneratedBy ECO_0000203 NP1008709.RA7H6G-HGmz8TwD85KX1NHz1VxOENvocOp7zIQqQ0bMe8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1008709.RA7H6G-HGmz8TwD85KX1NHz1VxOENvocOp7zIQqQ0bMe8130_provenance.