Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP541700.RAE5BMetUQUmacaTYlSQkfUl42LW4ZBSil4kceofvWNiQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP541700.RAE5BMetUQUmacaTYlSQkfUl42LW4ZBSil4kceofvWNiQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541700.RAE5BMetUQUmacaTYlSQkfUl42LW4ZBSil4kceofvWNiQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541700.RAE5BMetUQUmacaTYlSQkfUl42LW4ZBSil4kceofvWNiQ130_provenance.
- NP541700.RAE5BMetUQUmacaTYlSQkfUl42LW4ZBSil4kceofvWNiQ130_assertion description "[Progression was faster in patients with SCA2 mutations and normal alleles with 22 or fewer repeats (P = .02) and in patients with SCA3 mutations with parkinsonism and/or dystonia at baseline (P = .003).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541700.RAE5BMetUQUmacaTYlSQkfUl42LW4ZBSil4kceofvWNiQ130_provenance.
- NP541700.RAE5BMetUQUmacaTYlSQkfUl42LW4ZBSil4kceofvWNiQ130_assertion evidence source_evidence_literature NP541700.RAE5BMetUQUmacaTYlSQkfUl42LW4ZBSil4kceofvWNiQ130_provenance.
- NP541700.RAE5BMetUQUmacaTYlSQkfUl42LW4ZBSil4kceofvWNiQ130_assertion SIO_000772 22491195 NP541700.RAE5BMetUQUmacaTYlSQkfUl42LW4ZBSil4kceofvWNiQ130_provenance.
- NP541700.RAE5BMetUQUmacaTYlSQkfUl42LW4ZBSil4kceofvWNiQ130_assertion wasDerivedFrom befree-20150227 NP541700.RAE5BMetUQUmacaTYlSQkfUl42LW4ZBSil4kceofvWNiQ130_provenance.
- NP541700.RAE5BMetUQUmacaTYlSQkfUl42LW4ZBSil4kceofvWNiQ130_assertion wasGeneratedBy ECO_0000203 NP541700.RAE5BMetUQUmacaTYlSQkfUl42LW4ZBSil4kceofvWNiQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP541700.RAE5BMetUQUmacaTYlSQkfUl42LW4ZBSil4kceofvWNiQ130_provenance.