Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP615040.RAfWefmWW6u5q0PmrxyvPoXhK7CuuzRrR5DYEp9VN9wI0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615040.RAfWefmWW6u5q0PmrxyvPoXhK7CuuzRrR5DYEp9VN9wI0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615040.RAfWefmWW6u5q0PmrxyvPoXhK7CuuzRrR5DYEp9VN9wI0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615040.RAfWefmWW6u5q0PmrxyvPoXhK7CuuzRrR5DYEp9VN9wI0130_provenance.
- NP615040.RAfWefmWW6u5q0PmrxyvPoXhK7CuuzRrR5DYEp9VN9wI0130_assertion description "[A total of 108 patients from 54 families (38 apparently dominant [ADCA] and 16 apparently recessive) with adult-onset hereditary ataxia and 75 apparently sporadic patients were assessed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615040.RAfWefmWW6u5q0PmrxyvPoXhK7CuuzRrR5DYEp9VN9wI0130_provenance.
- NP615040.RAfWefmWW6u5q0PmrxyvPoXhK7CuuzRrR5DYEp9VN9wI0130_assertion evidence source_evidence_literature NP615040.RAfWefmWW6u5q0PmrxyvPoXhK7CuuzRrR5DYEp9VN9wI0130_provenance.
- NP615040.RAfWefmWW6u5q0PmrxyvPoXhK7CuuzRrR5DYEp9VN9wI0130_assertion SIO_000772 16149098 NP615040.RAfWefmWW6u5q0PmrxyvPoXhK7CuuzRrR5DYEp9VN9wI0130_provenance.
- NP615040.RAfWefmWW6u5q0PmrxyvPoXhK7CuuzRrR5DYEp9VN9wI0130_assertion wasDerivedFrom befree-20150227 NP615040.RAfWefmWW6u5q0PmrxyvPoXhK7CuuzRrR5DYEp9VN9wI0130_provenance.
- NP615040.RAfWefmWW6u5q0PmrxyvPoXhK7CuuzRrR5DYEp9VN9wI0130_assertion wasGeneratedBy ECO_0000203 NP615040.RAfWefmWW6u5q0PmrxyvPoXhK7CuuzRrR5DYEp9VN9wI0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP615040.RAfWefmWW6u5q0PmrxyvPoXhK7CuuzRrR5DYEp9VN9wI0130_provenance.