Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_provenance.
- NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_assertion description "[A mutation in this gene causes X-linked cone dystrophy/type of hereditary retinal degeneration is distinct from retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_provenance.
- NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_assertion evidence source_evidence_literature NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_provenance.
- NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_assertion SIO_000772 11875055 NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_provenance.
- NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_assertion wasDerivedFrom lhgdn-20090331 NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_provenance.
- NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_assertion wasGeneratedBy ECO_0000203 NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_provenance.