Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_provenance.
- NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_assertion description "[Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_provenance.
- NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_assertion evidence source_evidence_literature NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_provenance.
- NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_assertion SIO_000772 9112595 NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_provenance.
- NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_assertion wasDerivedFrom befree-20140225 NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_provenance.
- NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_assertion wasGeneratedBy ECO_0000203 NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP256409.RAIyrjX-shgABhc9W507dCyx0CT3oD-j4Qg8HTx6lUVJE130_provenance.