Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP223756.RARDxyWzQc-RR4kQBFGxqcw9AEtmWjruoGVHuqNDqhEWI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP223756.RARDxyWzQc-RR4kQBFGxqcw9AEtmWjruoGVHuqNDqhEWI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP223756.RARDxyWzQc-RR4kQBFGxqcw9AEtmWjruoGVHuqNDqhEWI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP223756.RARDxyWzQc-RR4kQBFGxqcw9AEtmWjruoGVHuqNDqhEWI130_provenance.
- NP223756.RARDxyWzQc-RR4kQBFGxqcw9AEtmWjruoGVHuqNDqhEWI130_assertion description "[Although clinical features associated with the T666M CACNA1A mutation are highly variable, downbeat positioning nystagmus may be an important clinical feature of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223756.RARDxyWzQc-RR4kQBFGxqcw9AEtmWjruoGVHuqNDqhEWI130_provenance.
- NP223756.RARDxyWzQc-RR4kQBFGxqcw9AEtmWjruoGVHuqNDqhEWI130_assertion evidence source_evidence_literature NP223756.RARDxyWzQc-RR4kQBFGxqcw9AEtmWjruoGVHuqNDqhEWI130_provenance.
- NP223756.RARDxyWzQc-RR4kQBFGxqcw9AEtmWjruoGVHuqNDqhEWI130_assertion SIO_000772 18670797 NP223756.RARDxyWzQc-RR4kQBFGxqcw9AEtmWjruoGVHuqNDqhEWI130_provenance.
- NP223756.RARDxyWzQc-RR4kQBFGxqcw9AEtmWjruoGVHuqNDqhEWI130_assertion wasDerivedFrom befree-20140225 NP223756.RARDxyWzQc-RR4kQBFGxqcw9AEtmWjruoGVHuqNDqhEWI130_provenance.
- NP223756.RARDxyWzQc-RR4kQBFGxqcw9AEtmWjruoGVHuqNDqhEWI130_assertion wasGeneratedBy ECO_0000203 NP223756.RARDxyWzQc-RR4kQBFGxqcw9AEtmWjruoGVHuqNDqhEWI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP223756.RARDxyWzQc-RR4kQBFGxqcw9AEtmWjruoGVHuqNDqhEWI130_provenance.