Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP689722.RA3xDPfjOO99EmQ_L-EUkhlpiI5bKBrZW8iYsYH-bbnKo130_assertion> ?p ?o ?g. }
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- NP689722.RA3xDPfjOO99EmQ_L-EUkhlpiI5bKBrZW8iYsYH-bbnKo130_assertion type Assertion NP689722.RA3xDPfjOO99EmQ_L-EUkhlpiI5bKBrZW8iYsYH-bbnKo130_head.
- NP689722.RA3xDPfjOO99EmQ_L-EUkhlpiI5bKBrZW8iYsYH-bbnKo130_assertion wasGeneratedBy ECO_0000203 NP689722.RA3xDPfjOO99EmQ_L-EUkhlpiI5bKBrZW8iYsYH-bbnKo130_provenance.
- NP689722.RA3xDPfjOO99EmQ_L-EUkhlpiI5bKBrZW8iYsYH-bbnKo130_assertion wasDerivedFrom befree-2016 NP689722.RA3xDPfjOO99EmQ_L-EUkhlpiI5bKBrZW8iYsYH-bbnKo130_provenance.
- NP689722.RA3xDPfjOO99EmQ_L-EUkhlpiI5bKBrZW8iYsYH-bbnKo130_assertion SIO_000772 18728015 NP689722.RA3xDPfjOO99EmQ_L-EUkhlpiI5bKBrZW8iYsYH-bbnKo130_provenance.
- NP689722.RA3xDPfjOO99EmQ_L-EUkhlpiI5bKBrZW8iYsYH-bbnKo130_assertion evidence source_evidence_literature NP689722.RA3xDPfjOO99EmQ_L-EUkhlpiI5bKBrZW8iYsYH-bbnKo130_provenance.
- NP689722.RA3xDPfjOO99EmQ_L-EUkhlpiI5bKBrZW8iYsYH-bbnKo130_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." NP689722.RA3xDPfjOO99EmQ_L-EUkhlpiI5bKBrZW8iYsYH-bbnKo130_provenance.