Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_provenance.
- NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_assertion description "[Using the Hereditary Hearing Loss arrayed primer extension (APEX) array, which contains 198 mutations across 8 hearing loss-associated genes (GJB2, GJB6, GJB3, GJA1, SLC26A4, SLC26A5, 12S-rRNA, and tRNA Ser), we compared the frequency of sequence variants in 94 individuals with early presbycusis to 50 unaffected controls and aimed to identify possible genetic contributors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_provenance.
- NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_assertion evidence source_evidence_literature NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_provenance.
- NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_assertion SIO_000772 18988928 NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_provenance.
- NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_assertion wasDerivedFrom befree-20140225 NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_provenance.
- NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_assertion wasGeneratedBy ECO_0000203 NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_provenance.