Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP569.RAATl1Dp8WTYgV6kLlrpspUF8E51Y8wYKSzIkcdMP_fX8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP569.RAATl1Dp8WTYgV6kLlrpspUF8E51Y8wYKSzIkcdMP_fX8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP569.RAATl1Dp8WTYgV6kLlrpspUF8E51Y8wYKSzIkcdMP_fX8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP569.RAATl1Dp8WTYgV6kLlrpspUF8E51Y8wYKSzIkcdMP_fX8130_provenance.
- NP569.RAATl1Dp8WTYgV6kLlrpspUF8E51Y8wYKSzIkcdMP_fX8130_assertion description "[Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569.RAATl1Dp8WTYgV6kLlrpspUF8E51Y8wYKSzIkcdMP_fX8130_provenance.
- NP569.RAATl1Dp8WTYgV6kLlrpspUF8E51Y8wYKSzIkcdMP_fX8130_assertion evidence source_evidence_curated NP569.RAATl1Dp8WTYgV6kLlrpspUF8E51Y8wYKSzIkcdMP_fX8130_provenance.
- NP569.RAATl1Dp8WTYgV6kLlrpspUF8E51Y8wYKSzIkcdMP_fX8130_assertion SIO_000772 15174025 NP569.RAATl1Dp8WTYgV6kLlrpspUF8E51Y8wYKSzIkcdMP_fX8130_provenance.
- NP569.RAATl1Dp8WTYgV6kLlrpspUF8E51Y8wYKSzIkcdMP_fX8130_assertion wasDerivedFrom uniprot-20130724 NP569.RAATl1Dp8WTYgV6kLlrpspUF8E51Y8wYKSzIkcdMP_fX8130_provenance.
- NP569.RAATl1Dp8WTYgV6kLlrpspUF8E51Y8wYKSzIkcdMP_fX8130_assertion wasGeneratedBy ECO_0000218 NP569.RAATl1Dp8WTYgV6kLlrpspUF8E51Y8wYKSzIkcdMP_fX8130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP569.RAATl1Dp8WTYgV6kLlrpspUF8E51Y8wYKSzIkcdMP_fX8130_provenance.