Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP887067.RAQMZmdJQSvnl8P0j9y2IpkGu5fPfpZ7H8AlsfFyXkxlM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887067.RAQMZmdJQSvnl8P0j9y2IpkGu5fPfpZ7H8AlsfFyXkxlM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887067.RAQMZmdJQSvnl8P0j9y2IpkGu5fPfpZ7H8AlsfFyXkxlM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887067.RAQMZmdJQSvnl8P0j9y2IpkGu5fPfpZ7H8AlsfFyXkxlM130_provenance.
- NP887067.RAQMZmdJQSvnl8P0j9y2IpkGu5fPfpZ7H8AlsfFyXkxlM130_assertion description "[Mutations in the MYO7A gene cause a deaf-blindness disorder, known as Usher syndrome 1B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887067.RAQMZmdJQSvnl8P0j9y2IpkGu5fPfpZ7H8AlsfFyXkxlM130_provenance.
- NP887067.RAQMZmdJQSvnl8P0j9y2IpkGu5fPfpZ7H8AlsfFyXkxlM130_assertion evidence source_evidence_literature NP887067.RAQMZmdJQSvnl8P0j9y2IpkGu5fPfpZ7H8AlsfFyXkxlM130_provenance.
- NP887067.RAQMZmdJQSvnl8P0j9y2IpkGu5fPfpZ7H8AlsfFyXkxlM130_assertion SIO_000772 21493626 NP887067.RAQMZmdJQSvnl8P0j9y2IpkGu5fPfpZ7H8AlsfFyXkxlM130_provenance.
- NP887067.RAQMZmdJQSvnl8P0j9y2IpkGu5fPfpZ7H8AlsfFyXkxlM130_assertion wasDerivedFrom befree-2016 NP887067.RAQMZmdJQSvnl8P0j9y2IpkGu5fPfpZ7H8AlsfFyXkxlM130_provenance.
- NP887067.RAQMZmdJQSvnl8P0j9y2IpkGu5fPfpZ7H8AlsfFyXkxlM130_assertion wasGeneratedBy ECO_0000203 NP887067.RAQMZmdJQSvnl8P0j9y2IpkGu5fPfpZ7H8AlsfFyXkxlM130_provenance.
- befree-2016 importedOn "2016-02-19" NP887067.RAQMZmdJQSvnl8P0j9y2IpkGu5fPfpZ7H8AlsfFyXkxlM130_provenance.