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- source_evidence_literature type ECO_0000212 NP933095.RArOh9Nvkn2xS41-iBrYfTY-6tUbMp73Vojao30izMMpk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP933095.RArOh9Nvkn2xS41-iBrYfTY-6tUbMp73Vojao30izMMpk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP933095.RArOh9Nvkn2xS41-iBrYfTY-6tUbMp73Vojao30izMMpk130_provenance.
- NP933095.RArOh9Nvkn2xS41-iBrYfTY-6tUbMp73Vojao30izMMpk130_assertion description "[Independently, we also identified compound heterozygous WDR19 mutations by exome sequencing in a Moroccan family with isolated nephronophthisis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933095.RArOh9Nvkn2xS41-iBrYfTY-6tUbMp73Vojao30izMMpk130_provenance.
- NP933095.RArOh9Nvkn2xS41-iBrYfTY-6tUbMp73Vojao30izMMpk130_assertion evidence source_evidence_literature NP933095.RArOh9Nvkn2xS41-iBrYfTY-6tUbMp73Vojao30izMMpk130_provenance.
- NP933095.RArOh9Nvkn2xS41-iBrYfTY-6tUbMp73Vojao30izMMpk130_assertion SIO_000772 22019273 NP933095.RArOh9Nvkn2xS41-iBrYfTY-6tUbMp73Vojao30izMMpk130_provenance.
- NP933095.RArOh9Nvkn2xS41-iBrYfTY-6tUbMp73Vojao30izMMpk130_assertion wasDerivedFrom befree-20150227 NP933095.RArOh9Nvkn2xS41-iBrYfTY-6tUbMp73Vojao30izMMpk130_provenance.
- NP933095.RArOh9Nvkn2xS41-iBrYfTY-6tUbMp73Vojao30izMMpk130_assertion wasGeneratedBy ECO_0000203 NP933095.RArOh9Nvkn2xS41-iBrYfTY-6tUbMp73Vojao30izMMpk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP933095.RArOh9Nvkn2xS41-iBrYfTY-6tUbMp73Vojao30izMMpk130_provenance.