Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_provenance.
- NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_assertion description "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_provenance.
- NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_assertion evidence source_evidence_literature NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_provenance.
- NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_assertion SIO_000772 10502787 NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_provenance.
- NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_assertion wasDerivedFrom befree-2016 NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_provenance.
- NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_assertion wasGeneratedBy ECO_0000203 NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_provenance.
- befree-2016 importedOn "2016-02-19" NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_provenance.