Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP887836.RAMyMPXzVVjPPUPDNKX6M7fZ3lOrf5tk5QtZ0MH-PrbQk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887836.RAMyMPXzVVjPPUPDNKX6M7fZ3lOrf5tk5QtZ0MH-PrbQk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887836.RAMyMPXzVVjPPUPDNKX6M7fZ3lOrf5tk5QtZ0MH-PrbQk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887836.RAMyMPXzVVjPPUPDNKX6M7fZ3lOrf5tk5QtZ0MH-PrbQk130_provenance.
- NP887836.RAMyMPXzVVjPPUPDNKX6M7fZ3lOrf5tk5QtZ0MH-PrbQk130_assertion description "[The Rp1-Q662X allele produces a truncated Rp1 protein, and homozygous Rp1-Q662X mice experience a progressive photoreceptor degeneration characterized disorganization of photoreceptor outer segments.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887836.RAMyMPXzVVjPPUPDNKX6M7fZ3lOrf5tk5QtZ0MH-PrbQk130_provenance.
- NP887836.RAMyMPXzVVjPPUPDNKX6M7fZ3lOrf5tk5QtZ0MH-PrbQk130_assertion evidence source_evidence_literature NP887836.RAMyMPXzVVjPPUPDNKX6M7fZ3lOrf5tk5QtZ0MH-PrbQk130_provenance.
- NP887836.RAMyMPXzVVjPPUPDNKX6M7fZ3lOrf5tk5QtZ0MH-PrbQk130_assertion SIO_000772 22927954 NP887836.RAMyMPXzVVjPPUPDNKX6M7fZ3lOrf5tk5QtZ0MH-PrbQk130_provenance.
- NP887836.RAMyMPXzVVjPPUPDNKX6M7fZ3lOrf5tk5QtZ0MH-PrbQk130_assertion wasDerivedFrom befree-20140225 NP887836.RAMyMPXzVVjPPUPDNKX6M7fZ3lOrf5tk5QtZ0MH-PrbQk130_provenance.
- NP887836.RAMyMPXzVVjPPUPDNKX6M7fZ3lOrf5tk5QtZ0MH-PrbQk130_assertion wasGeneratedBy ECO_0000203 NP887836.RAMyMPXzVVjPPUPDNKX6M7fZ3lOrf5tk5QtZ0MH-PrbQk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP887836.RAMyMPXzVVjPPUPDNKX6M7fZ3lOrf5tk5QtZ0MH-PrbQk130_provenance.