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- source_evidence_literature type ECO_0000212 NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_provenance.
- NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_assertion description "[Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_provenance.
- NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_assertion evidence source_evidence_literature NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_provenance.
- NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_assertion SIO_000772 11090341 NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_provenance.
- NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_assertion wasDerivedFrom befree-20150227 NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_provenance.
- NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_assertion wasGeneratedBy ECO_0000203 NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_provenance.