Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1244141.RAH5nxwQ7IJ15h6NZ2YvooN1uvtS6f1gOeBkk2CRrAkTw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1244141.RAH5nxwQ7IJ15h6NZ2YvooN1uvtS6f1gOeBkk2CRrAkTw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1244141.RAH5nxwQ7IJ15h6NZ2YvooN1uvtS6f1gOeBkk2CRrAkTw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1244141.RAH5nxwQ7IJ15h6NZ2YvooN1uvtS6f1gOeBkk2CRrAkTw130_provenance.
- NP1244141.RAH5nxwQ7IJ15h6NZ2YvooN1uvtS6f1gOeBkk2CRrAkTw130_assertion description "[We hereby screened for the presence of the C9ORF72 hexanucleotide repeat expansion in 331 patients with multiple system atrophy-cerebellar variant and 98 unrelated patients with molecularly un-assigned spinocerebellar ataxia in Taiwan utilizing a repeat-primed polymerase chain reaction assay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244141.RAH5nxwQ7IJ15h6NZ2YvooN1uvtS6f1gOeBkk2CRrAkTw130_provenance.
- NP1244141.RAH5nxwQ7IJ15h6NZ2YvooN1uvtS6f1gOeBkk2CRrAkTw130_assertion evidence source_evidence_literature NP1244141.RAH5nxwQ7IJ15h6NZ2YvooN1uvtS6f1gOeBkk2CRrAkTw130_provenance.
- NP1244141.RAH5nxwQ7IJ15h6NZ2YvooN1uvtS6f1gOeBkk2CRrAkTw130_assertion SIO_000772 25467142 NP1244141.RAH5nxwQ7IJ15h6NZ2YvooN1uvtS6f1gOeBkk2CRrAkTw130_provenance.
- NP1244141.RAH5nxwQ7IJ15h6NZ2YvooN1uvtS6f1gOeBkk2CRrAkTw130_assertion wasDerivedFrom befree-2016 NP1244141.RAH5nxwQ7IJ15h6NZ2YvooN1uvtS6f1gOeBkk2CRrAkTw130_provenance.
- NP1244141.RAH5nxwQ7IJ15h6NZ2YvooN1uvtS6f1gOeBkk2CRrAkTw130_assertion wasGeneratedBy ECO_0000203 NP1244141.RAH5nxwQ7IJ15h6NZ2YvooN1uvtS6f1gOeBkk2CRrAkTw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1244141.RAH5nxwQ7IJ15h6NZ2YvooN1uvtS6f1gOeBkk2CRrAkTw130_provenance.