Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478752.RAbuf2x0GGy41nCtMrnzdPf6twwjICwGpwcrKiMOBNPxc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478752.RAbuf2x0GGy41nCtMrnzdPf6twwjICwGpwcrKiMOBNPxc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478752.RAbuf2x0GGy41nCtMrnzdPf6twwjICwGpwcrKiMOBNPxc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478752.RAbuf2x0GGy41nCtMrnzdPf6twwjICwGpwcrKiMOBNPxc130_provenance.
- NP478752.RAbuf2x0GGy41nCtMrnzdPf6twwjICwGpwcrKiMOBNPxc130_assertion description "[Extensive mutational analysis of PRKCSH and SEC63 broadens the spectrum of polycystic liver disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478752.RAbuf2x0GGy41nCtMrnzdPf6twwjICwGpwcrKiMOBNPxc130_provenance.
- NP478752.RAbuf2x0GGy41nCtMrnzdPf6twwjICwGpwcrKiMOBNPxc130_assertion evidence source_evidence_literature NP478752.RAbuf2x0GGy41nCtMrnzdPf6twwjICwGpwcrKiMOBNPxc130_provenance.
- NP478752.RAbuf2x0GGy41nCtMrnzdPf6twwjICwGpwcrKiMOBNPxc130_assertion SIO_000772 16835903 NP478752.RAbuf2x0GGy41nCtMrnzdPf6twwjICwGpwcrKiMOBNPxc130_provenance.
- NP478752.RAbuf2x0GGy41nCtMrnzdPf6twwjICwGpwcrKiMOBNPxc130_assertion wasDerivedFrom befree-20140225 NP478752.RAbuf2x0GGy41nCtMrnzdPf6twwjICwGpwcrKiMOBNPxc130_provenance.
- NP478752.RAbuf2x0GGy41nCtMrnzdPf6twwjICwGpwcrKiMOBNPxc130_assertion wasGeneratedBy ECO_0000203 NP478752.RAbuf2x0GGy41nCtMrnzdPf6twwjICwGpwcrKiMOBNPxc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478752.RAbuf2x0GGy41nCtMrnzdPf6twwjICwGpwcrKiMOBNPxc130_provenance.