Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_provenance.
- NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_assertion description "[Mutations in VLGRI in humans result in one form (2C) of Usher syndrome, the most common genetic cause of combined blindness and deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_provenance.
- NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_assertion evidence source_evidence_literature NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_provenance.
- NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_assertion SIO_000772 21618827 NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_provenance.
- NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_assertion wasDerivedFrom befree-20150227 NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_provenance.
- NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_assertion wasGeneratedBy ECO_0000203 NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_provenance.