Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_provenance.
- NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_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." NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_provenance.
- NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_assertion evidence source_evidence_literature NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_provenance.
- NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_assertion SIO_000772 17049295 NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_provenance.
- NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_assertion wasDerivedFrom lhgdn-20090331 NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_provenance.
- NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_assertion wasGeneratedBy ECO_0000203 NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_provenance.