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- source_evidence_literature type ECO_0000212 NP1008702.RAnJWNm0xnzT-b6yal4G_zc1jVXD41sESTilsaSSLfj6g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1008702.RAnJWNm0xnzT-b6yal4G_zc1jVXD41sESTilsaSSLfj6g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1008702.RAnJWNm0xnzT-b6yal4G_zc1jVXD41sESTilsaSSLfj6g130_provenance.
- NP1008702.RAnJWNm0xnzT-b6yal4G_zc1jVXD41sESTilsaSSLfj6g130_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." NP1008702.RAnJWNm0xnzT-b6yal4G_zc1jVXD41sESTilsaSSLfj6g130_provenance.
- NP1008702.RAnJWNm0xnzT-b6yal4G_zc1jVXD41sESTilsaSSLfj6g130_assertion evidence source_evidence_literature NP1008702.RAnJWNm0xnzT-b6yal4G_zc1jVXD41sESTilsaSSLfj6g130_provenance.
- NP1008702.RAnJWNm0xnzT-b6yal4G_zc1jVXD41sESTilsaSSLfj6g130_assertion SIO_000772 22929189 NP1008702.RAnJWNm0xnzT-b6yal4G_zc1jVXD41sESTilsaSSLfj6g130_provenance.
- NP1008702.RAnJWNm0xnzT-b6yal4G_zc1jVXD41sESTilsaSSLfj6g130_assertion wasDerivedFrom befree-2016 NP1008702.RAnJWNm0xnzT-b6yal4G_zc1jVXD41sESTilsaSSLfj6g130_provenance.
- NP1008702.RAnJWNm0xnzT-b6yal4G_zc1jVXD41sESTilsaSSLfj6g130_assertion wasGeneratedBy ECO_0000203 NP1008702.RAnJWNm0xnzT-b6yal4G_zc1jVXD41sESTilsaSSLfj6g130_provenance.
- befree-2016 importedOn "2016-02-19" NP1008702.RAnJWNm0xnzT-b6yal4G_zc1jVXD41sESTilsaSSLfj6g130_provenance.