Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP303664.RA9-6VvY5jAJNhtFr3SQUSFbymHl8rbqlLn5CPtxGB1mQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP303664.RA9-6VvY5jAJNhtFr3SQUSFbymHl8rbqlLn5CPtxGB1mQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP303664.RA9-6VvY5jAJNhtFr3SQUSFbymHl8rbqlLn5CPtxGB1mQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP303664.RA9-6VvY5jAJNhtFr3SQUSFbymHl8rbqlLn5CPtxGB1mQ130_provenance.
- NP303664.RA9-6VvY5jAJNhtFr3SQUSFbymHl8rbqlLn5CPtxGB1mQ130_assertion description "[ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303664.RA9-6VvY5jAJNhtFr3SQUSFbymHl8rbqlLn5CPtxGB1mQ130_provenance.
- NP303664.RA9-6VvY5jAJNhtFr3SQUSFbymHl8rbqlLn5CPtxGB1mQ130_assertion evidence source_evidence_literature NP303664.RA9-6VvY5jAJNhtFr3SQUSFbymHl8rbqlLn5CPtxGB1mQ130_provenance.
- NP303664.RA9-6VvY5jAJNhtFr3SQUSFbymHl8rbqlLn5CPtxGB1mQ130_assertion SIO_000772 23867502 NP303664.RA9-6VvY5jAJNhtFr3SQUSFbymHl8rbqlLn5CPtxGB1mQ130_provenance.
- NP303664.RA9-6VvY5jAJNhtFr3SQUSFbymHl8rbqlLn5CPtxGB1mQ130_assertion wasDerivedFrom befree-20140225 NP303664.RA9-6VvY5jAJNhtFr3SQUSFbymHl8rbqlLn5CPtxGB1mQ130_provenance.
- NP303664.RA9-6VvY5jAJNhtFr3SQUSFbymHl8rbqlLn5CPtxGB1mQ130_assertion wasGeneratedBy ECO_0000203 NP303664.RA9-6VvY5jAJNhtFr3SQUSFbymHl8rbqlLn5CPtxGB1mQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP303664.RA9-6VvY5jAJNhtFr3SQUSFbymHl8rbqlLn5CPtxGB1mQ130_provenance.