Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP761450.RAAYssPvlJoqUhSgDyzev1TYY_zTBmbyDSMpv_L9zHBZw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP761450.RAAYssPvlJoqUhSgDyzev1TYY_zTBmbyDSMpv_L9zHBZw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761450.RAAYssPvlJoqUhSgDyzev1TYY_zTBmbyDSMpv_L9zHBZw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761450.RAAYssPvlJoqUhSgDyzev1TYY_zTBmbyDSMpv_L9zHBZw130_provenance.
- befree-2016 importedOn "2016-02-19" NP761450.RAAYssPvlJoqUhSgDyzev1TYY_zTBmbyDSMpv_L9zHBZw130_provenance.
- NP761450.RAAYssPvlJoqUhSgDyzev1TYY_zTBmbyDSMpv_L9zHBZw130_assertion wasGeneratedBy ECO_0000203 NP761450.RAAYssPvlJoqUhSgDyzev1TYY_zTBmbyDSMpv_L9zHBZw130_provenance.
- NP761450.RAAYssPvlJoqUhSgDyzev1TYY_zTBmbyDSMpv_L9zHBZw130_assertion wasDerivedFrom befree-2016 NP761450.RAAYssPvlJoqUhSgDyzev1TYY_zTBmbyDSMpv_L9zHBZw130_provenance.
- NP761450.RAAYssPvlJoqUhSgDyzev1TYY_zTBmbyDSMpv_L9zHBZw130_assertion SIO_000772 19732866 NP761450.RAAYssPvlJoqUhSgDyzev1TYY_zTBmbyDSMpv_L9zHBZw130_provenance.
- NP761450.RAAYssPvlJoqUhSgDyzev1TYY_zTBmbyDSMpv_L9zHBZw130_assertion evidence source_evidence_literature NP761450.RAAYssPvlJoqUhSgDyzev1TYY_zTBmbyDSMpv_L9zHBZw130_provenance.
- NP761450.RAAYssPvlJoqUhSgDyzev1TYY_zTBmbyDSMpv_L9zHBZw130_assertion description "[We identified an inherited brain-specific folate transport defect that is caused by mutations in the folate receptor 1 (FOLR1) gene coding for folate receptor alpha (FRalpha).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761450.RAAYssPvlJoqUhSgDyzev1TYY_zTBmbyDSMpv_L9zHBZw130_provenance.