Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP918338.RArCC3VbDBZ24DIOFyHGdHPI_bc3fRx7vzqIOPteYQD9s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP918338.RArCC3VbDBZ24DIOFyHGdHPI_bc3fRx7vzqIOPteYQD9s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP918338.RArCC3VbDBZ24DIOFyHGdHPI_bc3fRx7vzqIOPteYQD9s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP918338.RArCC3VbDBZ24DIOFyHGdHPI_bc3fRx7vzqIOPteYQD9s130_provenance.
- NP918338.RArCC3VbDBZ24DIOFyHGdHPI_bc3fRx7vzqIOPteYQD9s130_assertion description "[Mutations in RPGR account for over 70% of X-linked retinitis pigmentosa (XlRP), characterized by retinal degeneration and eventual blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918338.RArCC3VbDBZ24DIOFyHGdHPI_bc3fRx7vzqIOPteYQD9s130_provenance.
- NP918338.RArCC3VbDBZ24DIOFyHGdHPI_bc3fRx7vzqIOPteYQD9s130_assertion evidence source_evidence_literature NP918338.RArCC3VbDBZ24DIOFyHGdHPI_bc3fRx7vzqIOPteYQD9s130_provenance.
- NP918338.RArCC3VbDBZ24DIOFyHGdHPI_bc3fRx7vzqIOPteYQD9s130_assertion SIO_000772 21857984 NP918338.RArCC3VbDBZ24DIOFyHGdHPI_bc3fRx7vzqIOPteYQD9s130_provenance.
- NP918338.RArCC3VbDBZ24DIOFyHGdHPI_bc3fRx7vzqIOPteYQD9s130_assertion wasDerivedFrom befree-2016 NP918338.RArCC3VbDBZ24DIOFyHGdHPI_bc3fRx7vzqIOPteYQD9s130_provenance.
- NP918338.RArCC3VbDBZ24DIOFyHGdHPI_bc3fRx7vzqIOPteYQD9s130_assertion wasGeneratedBy ECO_0000203 NP918338.RArCC3VbDBZ24DIOFyHGdHPI_bc3fRx7vzqIOPteYQD9s130_provenance.
- befree-2016 importedOn "2016-02-19" NP918338.RArCC3VbDBZ24DIOFyHGdHPI_bc3fRx7vzqIOPteYQD9s130_provenance.