Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_provenance.
- NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_assertion description "[A primary role of the ABCA4 gene in STGD1/FFM and AR CRD, together with the gene's involvement in an as-yet-unknown proportion of cases with AR RP, strengthens the idea that mutations in the ABCA4 gene could be the most frequent cause of inherited retinal dystrophy in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_provenance.
- NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_assertion evidence source_evidence_literature NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_provenance.
- NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_assertion SIO_000772 10958761 NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_provenance.
- NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_assertion wasDerivedFrom befree-2016 NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_provenance.
- NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_assertion wasGeneratedBy ECO_0000203 NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_provenance.
- befree-2016 importedOn "2016-02-19" NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_provenance.