Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance.
- NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance.
- NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_assertion evidence source_evidence_literature NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance.
- NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_assertion SIO_000772 12687499 NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance.
- NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_assertion wasDerivedFrom befree-20150227 NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance.
- NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_assertion wasGeneratedBy ECO_0000203 NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance.