Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP646108.RAqAIjb_4E9RRtbMR_A2syy3hWnwt_GyOG3Q-OVw5d_XQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP646108.RAqAIjb_4E9RRtbMR_A2syy3hWnwt_GyOG3Q-OVw5d_XQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP646108.RAqAIjb_4E9RRtbMR_A2syy3hWnwt_GyOG3Q-OVw5d_XQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP646108.RAqAIjb_4E9RRtbMR_A2syy3hWnwt_GyOG3Q-OVw5d_XQ130_provenance.
- NP646108.RAqAIjb_4E9RRtbMR_A2syy3hWnwt_GyOG3Q-OVw5d_XQ130_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." NP646108.RAqAIjb_4E9RRtbMR_A2syy3hWnwt_GyOG3Q-OVw5d_XQ130_provenance.
- NP646108.RAqAIjb_4E9RRtbMR_A2syy3hWnwt_GyOG3Q-OVw5d_XQ130_assertion evidence source_evidence_literature NP646108.RAqAIjb_4E9RRtbMR_A2syy3hWnwt_GyOG3Q-OVw5d_XQ130_provenance.
- NP646108.RAqAIjb_4E9RRtbMR_A2syy3hWnwt_GyOG3Q-OVw5d_XQ130_assertion SIO_000772 22929189 NP646108.RAqAIjb_4E9RRtbMR_A2syy3hWnwt_GyOG3Q-OVw5d_XQ130_provenance.
- NP646108.RAqAIjb_4E9RRtbMR_A2syy3hWnwt_GyOG3Q-OVw5d_XQ130_assertion wasDerivedFrom befree-20140225 NP646108.RAqAIjb_4E9RRtbMR_A2syy3hWnwt_GyOG3Q-OVw5d_XQ130_provenance.
- NP646108.RAqAIjb_4E9RRtbMR_A2syy3hWnwt_GyOG3Q-OVw5d_XQ130_assertion wasGeneratedBy ECO_0000203 NP646108.RAqAIjb_4E9RRtbMR_A2syy3hWnwt_GyOG3Q-OVw5d_XQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP646108.RAqAIjb_4E9RRtbMR_A2syy3hWnwt_GyOG3Q-OVw5d_XQ130_provenance.