Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_provenance.
- NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_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." NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_provenance.
- NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_assertion evidence source_evidence_literature NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_provenance.
- NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_assertion SIO_000772 11875055 NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_provenance.
- NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_assertion wasDerivedFrom lhgdn-20090331 NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_provenance.
- NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_assertion wasGeneratedBy ECO_0000203 NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_provenance.