Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP788417.RACq3maFAzPyyRA_SkzPkA0Wl_WVo4K2tvTBQ_OEe5DAA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788417.RACq3maFAzPyyRA_SkzPkA0Wl_WVo4K2tvTBQ_OEe5DAA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788417.RACq3maFAzPyyRA_SkzPkA0Wl_WVo4K2tvTBQ_OEe5DAA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788417.RACq3maFAzPyyRA_SkzPkA0Wl_WVo4K2tvTBQ_OEe5DAA130_provenance.
- NP788417.RACq3maFAzPyyRA_SkzPkA0Wl_WVo4K2tvTBQ_OEe5DAA130_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." NP788417.RACq3maFAzPyyRA_SkzPkA0Wl_WVo4K2tvTBQ_OEe5DAA130_provenance.
- NP788417.RACq3maFAzPyyRA_SkzPkA0Wl_WVo4K2tvTBQ_OEe5DAA130_assertion evidence source_evidence_literature NP788417.RACq3maFAzPyyRA_SkzPkA0Wl_WVo4K2tvTBQ_OEe5DAA130_provenance.
- NP788417.RACq3maFAzPyyRA_SkzPkA0Wl_WVo4K2tvTBQ_OEe5DAA130_assertion SIO_000772 22929189 NP788417.RACq3maFAzPyyRA_SkzPkA0Wl_WVo4K2tvTBQ_OEe5DAA130_provenance.
- NP788417.RACq3maFAzPyyRA_SkzPkA0Wl_WVo4K2tvTBQ_OEe5DAA130_assertion wasDerivedFrom befree-20150227 NP788417.RACq3maFAzPyyRA_SkzPkA0Wl_WVo4K2tvTBQ_OEe5DAA130_provenance.
- NP788417.RACq3maFAzPyyRA_SkzPkA0Wl_WVo4K2tvTBQ_OEe5DAA130_assertion wasGeneratedBy ECO_0000203 NP788417.RACq3maFAzPyyRA_SkzPkA0Wl_WVo4K2tvTBQ_OEe5DAA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP788417.RACq3maFAzPyyRA_SkzPkA0Wl_WVo4K2tvTBQ_OEe5DAA130_provenance.