Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP256086.RAGvn7AtI1eJicBttbNSu-iA1XRvRPQD0yMGVCnXHPgM8130_assertion> ?p ?o ?g. }
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- NP256086.RAGvn7AtI1eJicBttbNSu-iA1XRvRPQD0yMGVCnXHPgM8130_assertion type Assertion NP256086.RAGvn7AtI1eJicBttbNSu-iA1XRvRPQD0yMGVCnXHPgM8130_head.
- NP256086.RAGvn7AtI1eJicBttbNSu-iA1XRvRPQD0yMGVCnXHPgM8130_assertion wasGeneratedBy ECO_0000203 NP256086.RAGvn7AtI1eJicBttbNSu-iA1XRvRPQD0yMGVCnXHPgM8130_provenance.
- NP256086.RAGvn7AtI1eJicBttbNSu-iA1XRvRPQD0yMGVCnXHPgM8130_assertion wasDerivedFrom befree-20150227 NP256086.RAGvn7AtI1eJicBttbNSu-iA1XRvRPQD0yMGVCnXHPgM8130_provenance.
- NP256086.RAGvn7AtI1eJicBttbNSu-iA1XRvRPQD0yMGVCnXHPgM8130_assertion SIO_000772 23838748 NP256086.RAGvn7AtI1eJicBttbNSu-iA1XRvRPQD0yMGVCnXHPgM8130_provenance.
- NP256086.RAGvn7AtI1eJicBttbNSu-iA1XRvRPQD0yMGVCnXHPgM8130_assertion evidence source_evidence_literature NP256086.RAGvn7AtI1eJicBttbNSu-iA1XRvRPQD0yMGVCnXHPgM8130_provenance.
- NP256086.RAGvn7AtI1eJicBttbNSu-iA1XRvRPQD0yMGVCnXHPgM8130_assertion description "[We describe a four-generation Italian family with familial hemiplegic migraine (FHM) and epilepsy due to a novel ATP1A2 missense mutation (R1007W).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256086.RAGvn7AtI1eJicBttbNSu-iA1XRvRPQD0yMGVCnXHPgM8130_provenance.