Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_provenance.
- NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_assertion description "[In over 50% of cases the causative gene is CACNA1A (FHM1), which in some cases produces a phenotype with cerebellar signs, including ataxia and nystagmus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_provenance.
- NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_assertion evidence source_evidence_literature NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_provenance.
- NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_assertion SIO_000772 15459825 NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_provenance.
- NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_assertion wasDerivedFrom befree-2016 NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_provenance.
- NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_assertion wasGeneratedBy ECO_0000203 NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_provenance.
- befree-2016 importedOn "2016-02-19" NP462805.RAcRa5BQHQHQlBv3nlKW_36yGGVer5HMy2zPo0CEKJzEM130_provenance.