Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_provenance.
- NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_assertion description "[Mutations in LCA5 are a rare cause of childhood retinal dystrophy accounting for ?2% of disease in this cohort, and the majority of LCA5 mutations are likely null.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_provenance.
- NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_assertion evidence source_evidence_literature NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_provenance.
- NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_assertion SIO_000772 23946133 NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_provenance.
- NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_assertion wasDerivedFrom befree-2016 NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_provenance.
- NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_assertion wasGeneratedBy ECO_0000203 NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1102524.RAfuYOmKn09hl7kPlQwnPSh9uslPTRePpd45punUw-0Rg130_provenance.