Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP256075.RAD6ORGQUB4PPeQe2swABQCRCSZ8pbjQ50dMgg_LXeHQw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256075.RAD6ORGQUB4PPeQe2swABQCRCSZ8pbjQ50dMgg_LXeHQw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256075.RAD6ORGQUB4PPeQe2swABQCRCSZ8pbjQ50dMgg_LXeHQw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256075.RAD6ORGQUB4PPeQe2swABQCRCSZ8pbjQ50dMgg_LXeHQw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP256075.RAD6ORGQUB4PPeQe2swABQCRCSZ8pbjQ50dMgg_LXeHQw130_provenance.
- NP256075.RAD6ORGQUB4PPeQe2swABQCRCSZ8pbjQ50dMgg_LXeHQw130_assertion wasGeneratedBy ECO_0000203 NP256075.RAD6ORGQUB4PPeQe2swABQCRCSZ8pbjQ50dMgg_LXeHQw130_provenance.
- NP256075.RAD6ORGQUB4PPeQe2swABQCRCSZ8pbjQ50dMgg_LXeHQw130_assertion wasDerivedFrom befree-20150227 NP256075.RAD6ORGQUB4PPeQe2swABQCRCSZ8pbjQ50dMgg_LXeHQw130_provenance.
- NP256075.RAD6ORGQUB4PPeQe2swABQCRCSZ8pbjQ50dMgg_LXeHQw130_assertion SIO_000772 18728015 NP256075.RAD6ORGQUB4PPeQe2swABQCRCSZ8pbjQ50dMgg_LXeHQw130_provenance.
- NP256075.RAD6ORGQUB4PPeQe2swABQCRCSZ8pbjQ50dMgg_LXeHQw130_assertion evidence source_evidence_literature NP256075.RAD6ORGQUB4PPeQe2swABQCRCSZ8pbjQ50dMgg_LXeHQw130_provenance.
- NP256075.RAD6ORGQUB4PPeQe2swABQCRCSZ8pbjQ50dMgg_LXeHQw130_assertion description "[Mutations in ATP1A2, the gene coding for the Na(+)/K(+)-ATPase alpha(2)-subunit, are associated with both familial hemiplegic migraine and sporadic cases of hemiplegic migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256075.RAD6ORGQUB4PPeQe2swABQCRCSZ8pbjQ50dMgg_LXeHQw130_provenance.