Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP392872.RAOln1-Ylxz8toR1xTjkaap8UW6uMeh1JCXd4Ef6Q7tbc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP392872.RAOln1-Ylxz8toR1xTjkaap8UW6uMeh1JCXd4Ef6Q7tbc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP392872.RAOln1-Ylxz8toR1xTjkaap8UW6uMeh1JCXd4Ef6Q7tbc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP392872.RAOln1-Ylxz8toR1xTjkaap8UW6uMeh1JCXd4Ef6Q7tbc130_provenance.
- NP392872.RAOln1-Ylxz8toR1xTjkaap8UW6uMeh1JCXd4Ef6Q7tbc130_assertion description "[Mutations in the RDS gene, which encodes the photoreceptor glycoprotein peripherin, have been sought in families with autosomal dominant retinal dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392872.RAOln1-Ylxz8toR1xTjkaap8UW6uMeh1JCXd4Ef6Q7tbc130_provenance.
- NP392872.RAOln1-Ylxz8toR1xTjkaap8UW6uMeh1JCXd4Ef6Q7tbc130_assertion evidence source_evidence_literature NP392872.RAOln1-Ylxz8toR1xTjkaap8UW6uMeh1JCXd4Ef6Q7tbc130_provenance.
- NP392872.RAOln1-Ylxz8toR1xTjkaap8UW6uMeh1JCXd4Ef6Q7tbc130_assertion SIO_000772 8485576 NP392872.RAOln1-Ylxz8toR1xTjkaap8UW6uMeh1JCXd4Ef6Q7tbc130_provenance.
- NP392872.RAOln1-Ylxz8toR1xTjkaap8UW6uMeh1JCXd4Ef6Q7tbc130_assertion wasDerivedFrom befree-20140225 NP392872.RAOln1-Ylxz8toR1xTjkaap8UW6uMeh1JCXd4Ef6Q7tbc130_provenance.
- NP392872.RAOln1-Ylxz8toR1xTjkaap8UW6uMeh1JCXd4Ef6Q7tbc130_assertion wasGeneratedBy ECO_0000203 NP392872.RAOln1-Ylxz8toR1xTjkaap8UW6uMeh1JCXd4Ef6Q7tbc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP392872.RAOln1-Ylxz8toR1xTjkaap8UW6uMeh1JCXd4Ef6Q7tbc130_provenance.