Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP256049.RAlsQ8OQTEOTpbX_rI12axhrNcfA69Cqf-HnaqQkYoeac130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256049.RAlsQ8OQTEOTpbX_rI12axhrNcfA69Cqf-HnaqQkYoeac130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256049.RAlsQ8OQTEOTpbX_rI12axhrNcfA69Cqf-HnaqQkYoeac130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256049.RAlsQ8OQTEOTpbX_rI12axhrNcfA69Cqf-HnaqQkYoeac130_provenance.
- befree-20150227 importedOn "2015-02-27" NP256049.RAlsQ8OQTEOTpbX_rI12axhrNcfA69Cqf-HnaqQkYoeac130_provenance.
- NP256049.RAlsQ8OQTEOTpbX_rI12axhrNcfA69Cqf-HnaqQkYoeac130_assertion wasGeneratedBy ECO_0000203 NP256049.RAlsQ8OQTEOTpbX_rI12axhrNcfA69Cqf-HnaqQkYoeac130_provenance.
- NP256049.RAlsQ8OQTEOTpbX_rI12axhrNcfA69Cqf-HnaqQkYoeac130_assertion wasDerivedFrom befree-20150227 NP256049.RAlsQ8OQTEOTpbX_rI12axhrNcfA69Cqf-HnaqQkYoeac130_provenance.
- NP256049.RAlsQ8OQTEOTpbX_rI12axhrNcfA69Cqf-HnaqQkYoeac130_assertion SIO_000772 23030542 NP256049.RAlsQ8OQTEOTpbX_rI12axhrNcfA69Cqf-HnaqQkYoeac130_provenance.
- NP256049.RAlsQ8OQTEOTpbX_rI12axhrNcfA69Cqf-HnaqQkYoeac130_assertion evidence source_evidence_literature NP256049.RAlsQ8OQTEOTpbX_rI12axhrNcfA69Cqf-HnaqQkYoeac130_provenance.
- NP256049.RAlsQ8OQTEOTpbX_rI12axhrNcfA69Cqf-HnaqQkYoeac130_assertion description "[Genetic studies in the rare form of familial hemiplegic migraine have identified mutations in 3 genes (CACNA1A, ATP1A2, and SCN1A) encoding proteins involved in ion homeostasis and suggesting that other such genes may be involved in the more common forms of migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256049.RAlsQ8OQTEOTpbX_rI12axhrNcfA69Cqf-HnaqQkYoeac130_provenance.