Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP369036.RA408vA2o0SUaH8fsIYHzFBe-RSDLowBYbbiKdD25oAzc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP369036.RA408vA2o0SUaH8fsIYHzFBe-RSDLowBYbbiKdD25oAzc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP369036.RA408vA2o0SUaH8fsIYHzFBe-RSDLowBYbbiKdD25oAzc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP369036.RA408vA2o0SUaH8fsIYHzFBe-RSDLowBYbbiKdD25oAzc130_provenance.
- NP369036.RA408vA2o0SUaH8fsIYHzFBe-RSDLowBYbbiKdD25oAzc130_assertion description "[These observations suggest that inactivating defects within the VDR gene do not commonly contribute to the primary pathogenesis of severe refractory hyperparathyroidism in uremia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP369036.RA408vA2o0SUaH8fsIYHzFBe-RSDLowBYbbiKdD25oAzc130_provenance.
- NP369036.RA408vA2o0SUaH8fsIYHzFBe-RSDLowBYbbiKdD25oAzc130_assertion evidence source_evidence_literature NP369036.RA408vA2o0SUaH8fsIYHzFBe-RSDLowBYbbiKdD25oAzc130_provenance.
- NP369036.RA408vA2o0SUaH8fsIYHzFBe-RSDLowBYbbiKdD25oAzc130_assertion SIO_000772 10690903 NP369036.RA408vA2o0SUaH8fsIYHzFBe-RSDLowBYbbiKdD25oAzc130_provenance.
- NP369036.RA408vA2o0SUaH8fsIYHzFBe-RSDLowBYbbiKdD25oAzc130_assertion wasDerivedFrom befree-20140225 NP369036.RA408vA2o0SUaH8fsIYHzFBe-RSDLowBYbbiKdD25oAzc130_provenance.
- NP369036.RA408vA2o0SUaH8fsIYHzFBe-RSDLowBYbbiKdD25oAzc130_assertion wasGeneratedBy ECO_0000203 NP369036.RA408vA2o0SUaH8fsIYHzFBe-RSDLowBYbbiKdD25oAzc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP369036.RA408vA2o0SUaH8fsIYHzFBe-RSDLowBYbbiKdD25oAzc130_provenance.