Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP808714.RA9moTTu1yP1JGlqQrfDpSoeDFHTVM-YOseaLnFgsvdeA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP808714.RA9moTTu1yP1JGlqQrfDpSoeDFHTVM-YOseaLnFgsvdeA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP808714.RA9moTTu1yP1JGlqQrfDpSoeDFHTVM-YOseaLnFgsvdeA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP808714.RA9moTTu1yP1JGlqQrfDpSoeDFHTVM-YOseaLnFgsvdeA130_provenance.
- NP808714.RA9moTTu1yP1JGlqQrfDpSoeDFHTVM-YOseaLnFgsvdeA130_assertion description "[We believe RDP is unique and should be classified separately from other forms of hereditary dystonia-parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP808714.RA9moTTu1yP1JGlqQrfDpSoeDFHTVM-YOseaLnFgsvdeA130_provenance.
- NP808714.RA9moTTu1yP1JGlqQrfDpSoeDFHTVM-YOseaLnFgsvdeA130_assertion evidence source_evidence_literature NP808714.RA9moTTu1yP1JGlqQrfDpSoeDFHTVM-YOseaLnFgsvdeA130_provenance.
- NP808714.RA9moTTu1yP1JGlqQrfDpSoeDFHTVM-YOseaLnFgsvdeA130_assertion SIO_000772 8255463 NP808714.RA9moTTu1yP1JGlqQrfDpSoeDFHTVM-YOseaLnFgsvdeA130_provenance.
- NP808714.RA9moTTu1yP1JGlqQrfDpSoeDFHTVM-YOseaLnFgsvdeA130_assertion wasDerivedFrom befree-20140225 NP808714.RA9moTTu1yP1JGlqQrfDpSoeDFHTVM-YOseaLnFgsvdeA130_provenance.
- NP808714.RA9moTTu1yP1JGlqQrfDpSoeDFHTVM-YOseaLnFgsvdeA130_assertion wasGeneratedBy ECO_0000203 NP808714.RA9moTTu1yP1JGlqQrfDpSoeDFHTVM-YOseaLnFgsvdeA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP808714.RA9moTTu1yP1JGlqQrfDpSoeDFHTVM-YOseaLnFgsvdeA130_provenance.