Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_provenance.
- NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_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." NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_provenance.
- NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_assertion evidence source_evidence_literature NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_provenance.
- NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_assertion SIO_000772 17049295 NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_provenance.
- NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_assertion wasDerivedFrom lhgdn-20090331 NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_provenance.
- NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_assertion wasGeneratedBy ECO_0000203 NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_provenance.