Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_provenance.
- NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_assertion description "[The discovery that the mouse shaker1 (Myo7(ash1)) locus encodes myosin VIIA led immediately to the identification of mutations in this gene in Usher syndrome type 1B; subsequently, mutations in this gene were also found associated with recessive and dominant nonsyndromic hearing loss (DFNB2 and DFNA11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_provenance.
- NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_assertion evidence source_evidence_literature NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_provenance.
- NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_assertion SIO_000772 10704189 NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_provenance.
- NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_assertion wasDerivedFrom befree-20150227 NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_provenance.
- NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_assertion wasGeneratedBy ECO_0000203 NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_provenance.