Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP582814.RAh9QZUNUBMF6JRUiWSPnGB2QyI5599X_FHcw3NRS507I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP582814.RAh9QZUNUBMF6JRUiWSPnGB2QyI5599X_FHcw3NRS507I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP582814.RAh9QZUNUBMF6JRUiWSPnGB2QyI5599X_FHcw3NRS507I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP582814.RAh9QZUNUBMF6JRUiWSPnGB2QyI5599X_FHcw3NRS507I130_provenance.
- NP582814.RAh9QZUNUBMF6JRUiWSPnGB2QyI5599X_FHcw3NRS507I130_assertion description "[Mutations in the peripherin/RDS gene have been identified in families with various retinopathies including those affecting primarily the macula and those restricted to the retinal periphery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582814.RAh9QZUNUBMF6JRUiWSPnGB2QyI5599X_FHcw3NRS507I130_provenance.
- NP582814.RAh9QZUNUBMF6JRUiWSPnGB2QyI5599X_FHcw3NRS507I130_assertion evidence source_evidence_literature NP582814.RAh9QZUNUBMF6JRUiWSPnGB2QyI5599X_FHcw3NRS507I130_provenance.
- NP582814.RAh9QZUNUBMF6JRUiWSPnGB2QyI5599X_FHcw3NRS507I130_assertion SIO_000772 17148040 NP582814.RAh9QZUNUBMF6JRUiWSPnGB2QyI5599X_FHcw3NRS507I130_provenance.
- NP582814.RAh9QZUNUBMF6JRUiWSPnGB2QyI5599X_FHcw3NRS507I130_assertion wasDerivedFrom befree-2016 NP582814.RAh9QZUNUBMF6JRUiWSPnGB2QyI5599X_FHcw3NRS507I130_provenance.
- NP582814.RAh9QZUNUBMF6JRUiWSPnGB2QyI5599X_FHcw3NRS507I130_assertion wasGeneratedBy ECO_0000203 NP582814.RAh9QZUNUBMF6JRUiWSPnGB2QyI5599X_FHcw3NRS507I130_provenance.
- befree-2016 importedOn "2016-02-19" NP582814.RAh9QZUNUBMF6JRUiWSPnGB2QyI5599X_FHcw3NRS507I130_provenance.