Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP690036.RAcKb8wX9EA4b9bFFAx3oYEJp-T9Qr3hRepiyRoFkQpWU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP690036.RAcKb8wX9EA4b9bFFAx3oYEJp-T9Qr3hRepiyRoFkQpWU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690036.RAcKb8wX9EA4b9bFFAx3oYEJp-T9Qr3hRepiyRoFkQpWU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690036.RAcKb8wX9EA4b9bFFAx3oYEJp-T9Qr3hRepiyRoFkQpWU130_provenance.
- NP690036.RAcKb8wX9EA4b9bFFAx3oYEJp-T9Qr3hRepiyRoFkQpWU130_assertion description "[In these cases, mutational analysis of the GCH1 gene is an alternative to diagnose DRD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690036.RAcKb8wX9EA4b9bFFAx3oYEJp-T9Qr3hRepiyRoFkQpWU130_provenance.
- NP690036.RAcKb8wX9EA4b9bFFAx3oYEJp-T9Qr3hRepiyRoFkQpWU130_assertion evidence source_evidence_literature NP690036.RAcKb8wX9EA4b9bFFAx3oYEJp-T9Qr3hRepiyRoFkQpWU130_provenance.
- NP690036.RAcKb8wX9EA4b9bFFAx3oYEJp-T9Qr3hRepiyRoFkQpWU130_assertion SIO_000772 18752196 NP690036.RAcKb8wX9EA4b9bFFAx3oYEJp-T9Qr3hRepiyRoFkQpWU130_provenance.
- NP690036.RAcKb8wX9EA4b9bFFAx3oYEJp-T9Qr3hRepiyRoFkQpWU130_assertion wasDerivedFrom befree-2016 NP690036.RAcKb8wX9EA4b9bFFAx3oYEJp-T9Qr3hRepiyRoFkQpWU130_provenance.
- NP690036.RAcKb8wX9EA4b9bFFAx3oYEJp-T9Qr3hRepiyRoFkQpWU130_assertion wasGeneratedBy ECO_0000203 NP690036.RAcKb8wX9EA4b9bFFAx3oYEJp-T9Qr3hRepiyRoFkQpWU130_provenance.
- befree-2016 importedOn "2016-02-19" NP690036.RAcKb8wX9EA4b9bFFAx3oYEJp-T9Qr3hRepiyRoFkQpWU130_provenance.