Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP323600.RAQHsTDeOVdz13yfK8ojX2w2rv2Tj5aGSfhAk4_3N1VaA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP323600.RAQHsTDeOVdz13yfK8ojX2w2rv2Tj5aGSfhAk4_3N1VaA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323600.RAQHsTDeOVdz13yfK8ojX2w2rv2Tj5aGSfhAk4_3N1VaA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323600.RAQHsTDeOVdz13yfK8ojX2w2rv2Tj5aGSfhAk4_3N1VaA130_provenance.
- NP323600.RAQHsTDeOVdz13yfK8ojX2w2rv2Tj5aGSfhAk4_3N1VaA130_assertion description "[Familial hemiplegic migraine is caused by CACNA1A missense mutations in 50% of families, including all families with cerebellar ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323600.RAQHsTDeOVdz13yfK8ojX2w2rv2Tj5aGSfhAk4_3N1VaA130_provenance.
- NP323600.RAQHsTDeOVdz13yfK8ojX2w2rv2Tj5aGSfhAk4_3N1VaA130_assertion evidence source_evidence_literature NP323600.RAQHsTDeOVdz13yfK8ojX2w2rv2Tj5aGSfhAk4_3N1VaA130_provenance.
- NP323600.RAQHsTDeOVdz13yfK8ojX2w2rv2Tj5aGSfhAk4_3N1VaA130_assertion SIO_000772 11061267 NP323600.RAQHsTDeOVdz13yfK8ojX2w2rv2Tj5aGSfhAk4_3N1VaA130_provenance.
- NP323600.RAQHsTDeOVdz13yfK8ojX2w2rv2Tj5aGSfhAk4_3N1VaA130_assertion wasDerivedFrom befree-20140225 NP323600.RAQHsTDeOVdz13yfK8ojX2w2rv2Tj5aGSfhAk4_3N1VaA130_provenance.
- NP323600.RAQHsTDeOVdz13yfK8ojX2w2rv2Tj5aGSfhAk4_3N1VaA130_assertion wasGeneratedBy ECO_0000203 NP323600.RAQHsTDeOVdz13yfK8ojX2w2rv2Tj5aGSfhAk4_3N1VaA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP323600.RAQHsTDeOVdz13yfK8ojX2w2rv2Tj5aGSfhAk4_3N1VaA130_provenance.