Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293914.RAy1c5m7Ba4d-X1LZCmu3htdsiF7-H3a32qFcsSAZ2woU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1293914.RAy1c5m7Ba4d-X1LZCmu3htdsiF7-H3a32qFcsSAZ2woU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293914.RAy1c5m7Ba4d-X1LZCmu3htdsiF7-H3a32qFcsSAZ2woU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293914.RAy1c5m7Ba4d-X1LZCmu3htdsiF7-H3a32qFcsSAZ2woU130_provenance.
- NP1293914.RAy1c5m7Ba4d-X1LZCmu3htdsiF7-H3a32qFcsSAZ2woU130_assertion description "[Thus, results of this large study do not support diagnostic screening of SCA2, SCA3, SCA6, and SCA17 gene repeats in the common idiopathic form of PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293914.RAy1c5m7Ba4d-X1LZCmu3htdsiF7-H3a32qFcsSAZ2woU130_provenance.
- NP1293914.RAy1c5m7Ba4d-X1LZCmu3htdsiF7-H3a32qFcsSAZ2woU130_assertion evidence source_evidence_literature NP1293914.RAy1c5m7Ba4d-X1LZCmu3htdsiF7-H3a32qFcsSAZ2woU130_provenance.
- NP1293914.RAy1c5m7Ba4d-X1LZCmu3htdsiF7-H3a32qFcsSAZ2woU130_assertion SIO_000772 26354989 NP1293914.RAy1c5m7Ba4d-X1LZCmu3htdsiF7-H3a32qFcsSAZ2woU130_provenance.
- NP1293914.RAy1c5m7Ba4d-X1LZCmu3htdsiF7-H3a32qFcsSAZ2woU130_assertion wasDerivedFrom befree-2016 NP1293914.RAy1c5m7Ba4d-X1LZCmu3htdsiF7-H3a32qFcsSAZ2woU130_provenance.
- NP1293914.RAy1c5m7Ba4d-X1LZCmu3htdsiF7-H3a32qFcsSAZ2woU130_assertion wasGeneratedBy ECO_0000203 NP1293914.RAy1c5m7Ba4d-X1LZCmu3htdsiF7-H3a32qFcsSAZ2woU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293914.RAy1c5m7Ba4d-X1LZCmu3htdsiF7-H3a32qFcsSAZ2woU130_provenance.