Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP463965.RAWRyVpX1nZ7vGGSkgORf1Iy9-qm3CBz9lhZzPQIpNVqI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP463965.RAWRyVpX1nZ7vGGSkgORf1Iy9-qm3CBz9lhZzPQIpNVqI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463965.RAWRyVpX1nZ7vGGSkgORf1Iy9-qm3CBz9lhZzPQIpNVqI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463965.RAWRyVpX1nZ7vGGSkgORf1Iy9-qm3CBz9lhZzPQIpNVqI130_provenance.
- NP463965.RAWRyVpX1nZ7vGGSkgORf1Iy9-qm3CBz9lhZzPQIpNVqI130_assertion description "[Detailed clinical descriptions and genetic analysis of patients with phenotypes intermediate between HPD/DRD (mild) and GCH-deficient HPA (severe) have not been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463965.RAWRyVpX1nZ7vGGSkgORf1Iy9-qm3CBz9lhZzPQIpNVqI130_provenance.
- NP463965.RAWRyVpX1nZ7vGGSkgORf1Iy9-qm3CBz9lhZzPQIpNVqI130_assertion evidence source_evidence_literature NP463965.RAWRyVpX1nZ7vGGSkgORf1Iy9-qm3CBz9lhZzPQIpNVqI130_provenance.
- NP463965.RAWRyVpX1nZ7vGGSkgORf1Iy9-qm3CBz9lhZzPQIpNVqI130_assertion SIO_000772 9667588 NP463965.RAWRyVpX1nZ7vGGSkgORf1Iy9-qm3CBz9lhZzPQIpNVqI130_provenance.
- NP463965.RAWRyVpX1nZ7vGGSkgORf1Iy9-qm3CBz9lhZzPQIpNVqI130_assertion wasDerivedFrom befree-20150227 NP463965.RAWRyVpX1nZ7vGGSkgORf1Iy9-qm3CBz9lhZzPQIpNVqI130_provenance.
- NP463965.RAWRyVpX1nZ7vGGSkgORf1Iy9-qm3CBz9lhZzPQIpNVqI130_assertion wasGeneratedBy ECO_0000203 NP463965.RAWRyVpX1nZ7vGGSkgORf1Iy9-qm3CBz9lhZzPQIpNVqI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP463965.RAWRyVpX1nZ7vGGSkgORf1Iy9-qm3CBz9lhZzPQIpNVqI130_provenance.