Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP271656.RAowm9sudI70lsX7jFIpuryo-CVUqJ1srQdS71gQ52wwk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP271656.RAowm9sudI70lsX7jFIpuryo-CVUqJ1srQdS71gQ52wwk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP271656.RAowm9sudI70lsX7jFIpuryo-CVUqJ1srQdS71gQ52wwk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP271656.RAowm9sudI70lsX7jFIpuryo-CVUqJ1srQdS71gQ52wwk130_provenance.
- NP271656.RAowm9sudI70lsX7jFIpuryo-CVUqJ1srQdS71gQ52wwk130_assertion description "[We report four novel mutations in peripherin/RDS and a relatively high frequency (23%) of mutations in this gene in families with adMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271656.RAowm9sudI70lsX7jFIpuryo-CVUqJ1srQdS71gQ52wwk130_provenance.
- NP271656.RAowm9sudI70lsX7jFIpuryo-CVUqJ1srQdS71gQ52wwk130_assertion evidence source_evidence_literature NP271656.RAowm9sudI70lsX7jFIpuryo-CVUqJ1srQdS71gQ52wwk130_provenance.
- NP271656.RAowm9sudI70lsX7jFIpuryo-CVUqJ1srQdS71gQ52wwk130_assertion SIO_000772 17653047 NP271656.RAowm9sudI70lsX7jFIpuryo-CVUqJ1srQdS71gQ52wwk130_provenance.
- NP271656.RAowm9sudI70lsX7jFIpuryo-CVUqJ1srQdS71gQ52wwk130_assertion wasDerivedFrom befree-20140225 NP271656.RAowm9sudI70lsX7jFIpuryo-CVUqJ1srQdS71gQ52wwk130_provenance.
- NP271656.RAowm9sudI70lsX7jFIpuryo-CVUqJ1srQdS71gQ52wwk130_assertion wasGeneratedBy ECO_0000203 NP271656.RAowm9sudI70lsX7jFIpuryo-CVUqJ1srQdS71gQ52wwk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP271656.RAowm9sudI70lsX7jFIpuryo-CVUqJ1srQdS71gQ52wwk130_provenance.