Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP889369.RAnPaQw6EHwWnB2IRRY-JnU5M2hvHg2iKLdVLC_v1xcsY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP889369.RAnPaQw6EHwWnB2IRRY-JnU5M2hvHg2iKLdVLC_v1xcsY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889369.RAnPaQw6EHwWnB2IRRY-JnU5M2hvHg2iKLdVLC_v1xcsY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889369.RAnPaQw6EHwWnB2IRRY-JnU5M2hvHg2iKLdVLC_v1xcsY130_provenance.
- NP889369.RAnPaQw6EHwWnB2IRRY-JnU5M2hvHg2iKLdVLC_v1xcsY130_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." NP889369.RAnPaQw6EHwWnB2IRRY-JnU5M2hvHg2iKLdVLC_v1xcsY130_provenance.
- NP889369.RAnPaQw6EHwWnB2IRRY-JnU5M2hvHg2iKLdVLC_v1xcsY130_assertion evidence source_evidence_literature NP889369.RAnPaQw6EHwWnB2IRRY-JnU5M2hvHg2iKLdVLC_v1xcsY130_provenance.
- NP889369.RAnPaQw6EHwWnB2IRRY-JnU5M2hvHg2iKLdVLC_v1xcsY130_assertion SIO_000772 22929189 NP889369.RAnPaQw6EHwWnB2IRRY-JnU5M2hvHg2iKLdVLC_v1xcsY130_provenance.
- NP889369.RAnPaQw6EHwWnB2IRRY-JnU5M2hvHg2iKLdVLC_v1xcsY130_assertion wasDerivedFrom befree-20140225 NP889369.RAnPaQw6EHwWnB2IRRY-JnU5M2hvHg2iKLdVLC_v1xcsY130_provenance.
- NP889369.RAnPaQw6EHwWnB2IRRY-JnU5M2hvHg2iKLdVLC_v1xcsY130_assertion wasGeneratedBy ECO_0000203 NP889369.RAnPaQw6EHwWnB2IRRY-JnU5M2hvHg2iKLdVLC_v1xcsY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP889369.RAnPaQw6EHwWnB2IRRY-JnU5M2hvHg2iKLdVLC_v1xcsY130_provenance.