Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP362531.RAlI-JUxm4jp2lX99GODNLK58kBlZKjxMSbjHiQ7he22U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP362531.RAlI-JUxm4jp2lX99GODNLK58kBlZKjxMSbjHiQ7he22U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP362531.RAlI-JUxm4jp2lX99GODNLK58kBlZKjxMSbjHiQ7he22U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP362531.RAlI-JUxm4jp2lX99GODNLK58kBlZKjxMSbjHiQ7he22U130_provenance.
- NP362531.RAlI-JUxm4jp2lX99GODNLK58kBlZKjxMSbjHiQ7he22U130_assertion wasGeneratedBy ECO_0000203 NP362531.RAlI-JUxm4jp2lX99GODNLK58kBlZKjxMSbjHiQ7he22U130_provenance.
- NP362531.RAlI-JUxm4jp2lX99GODNLK58kBlZKjxMSbjHiQ7he22U130_assertion wasDerivedFrom befree-20140225 NP362531.RAlI-JUxm4jp2lX99GODNLK58kBlZKjxMSbjHiQ7he22U130_provenance.
- NP362531.RAlI-JUxm4jp2lX99GODNLK58kBlZKjxMSbjHiQ7he22U130_assertion SIO_000772 10399872 NP362531.RAlI-JUxm4jp2lX99GODNLK58kBlZKjxMSbjHiQ7he22U130_provenance.
- NP362531.RAlI-JUxm4jp2lX99GODNLK58kBlZKjxMSbjHiQ7he22U130_assertion evidence source_evidence_literature NP362531.RAlI-JUxm4jp2lX99GODNLK58kBlZKjxMSbjHiQ7he22U130_provenance.
- NP362531.RAlI-JUxm4jp2lX99GODNLK58kBlZKjxMSbjHiQ7he22U130_assertion description "[We clinically and genetically evaluated 73 Italian families with autosomal dominant cerebellar ataxia (ADCA) type I. Spinocerebellar ataxia (SCA) type 1 was the most common genotype (SCA1), accounting for 41% of cases (30 families), SCA2 was slightly less frequent (29%, 21 families), and the remaining families were negative for the SCA1, SCA2, and SCA3 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362531.RAlI-JUxm4jp2lX99GODNLK58kBlZKjxMSbjHiQ7he22U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP362531.RAlI-JUxm4jp2lX99GODNLK58kBlZKjxMSbjHiQ7he22U130_provenance.