Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_provenance.
- NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_assertion description "[2 patients whose clinical features resembled those of multiple system atrophy of the cerebellar subtype (MSA-C) but without ocular motor apraxia and hypoalbuminemia/had a different nucleotide transition in the APTX gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_provenance.
- NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_assertion evidence source_evidence_literature NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_provenance.
- NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_assertion SIO_000772 17049295 NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_provenance.
- NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_assertion wasDerivedFrom lhgdn-20090331 NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_provenance.
- NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_assertion wasGeneratedBy ECO_0000203 NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_provenance.