Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP788419.RAfdI-ySrlGe_z33ocL3R1wu5CC2-gp-R_X1u1LaCSQBg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788419.RAfdI-ySrlGe_z33ocL3R1wu5CC2-gp-R_X1u1LaCSQBg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788419.RAfdI-ySrlGe_z33ocL3R1wu5CC2-gp-R_X1u1LaCSQBg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788419.RAfdI-ySrlGe_z33ocL3R1wu5CC2-gp-R_X1u1LaCSQBg130_provenance.
- NP788419.RAfdI-ySrlGe_z33ocL3R1wu5CC2-gp-R_X1u1LaCSQBg130_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." NP788419.RAfdI-ySrlGe_z33ocL3R1wu5CC2-gp-R_X1u1LaCSQBg130_provenance.
- NP788419.RAfdI-ySrlGe_z33ocL3R1wu5CC2-gp-R_X1u1LaCSQBg130_assertion evidence source_evidence_literature NP788419.RAfdI-ySrlGe_z33ocL3R1wu5CC2-gp-R_X1u1LaCSQBg130_provenance.
- NP788419.RAfdI-ySrlGe_z33ocL3R1wu5CC2-gp-R_X1u1LaCSQBg130_assertion SIO_000772 22929189 NP788419.RAfdI-ySrlGe_z33ocL3R1wu5CC2-gp-R_X1u1LaCSQBg130_provenance.
- NP788419.RAfdI-ySrlGe_z33ocL3R1wu5CC2-gp-R_X1u1LaCSQBg130_assertion wasDerivedFrom befree-20150227 NP788419.RAfdI-ySrlGe_z33ocL3R1wu5CC2-gp-R_X1u1LaCSQBg130_provenance.
- NP788419.RAfdI-ySrlGe_z33ocL3R1wu5CC2-gp-R_X1u1LaCSQBg130_assertion wasGeneratedBy ECO_0000203 NP788419.RAfdI-ySrlGe_z33ocL3R1wu5CC2-gp-R_X1u1LaCSQBg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP788419.RAfdI-ySrlGe_z33ocL3R1wu5CC2-gp-R_X1u1LaCSQBg130_provenance.