Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP363554.RALcltsaZPmXC_2IiDdy4YibMtFiOxpyj-4P6jmVjqBbQ130_assertion> ?p ?o ?g. }
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- NP363554.RALcltsaZPmXC_2IiDdy4YibMtFiOxpyj-4P6jmVjqBbQ130_assertion type Assertion NP363554.RALcltsaZPmXC_2IiDdy4YibMtFiOxpyj-4P6jmVjqBbQ130_head.
- NP363554.RALcltsaZPmXC_2IiDdy4YibMtFiOxpyj-4P6jmVjqBbQ130_assertion description "[Familial hemiplegic migraine (FHM) is genetically heterogeneous with mutations in the CACNA1A (FHM1), ATP1A2 (FHM2) and SCN1A (FHM3) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP363554.RALcltsaZPmXC_2IiDdy4YibMtFiOxpyj-4P6jmVjqBbQ130_provenance.
- NP363554.RALcltsaZPmXC_2IiDdy4YibMtFiOxpyj-4P6jmVjqBbQ130_assertion evidence source_evidence_literature NP363554.RALcltsaZPmXC_2IiDdy4YibMtFiOxpyj-4P6jmVjqBbQ130_provenance.
- NP363554.RALcltsaZPmXC_2IiDdy4YibMtFiOxpyj-4P6jmVjqBbQ130_assertion SIO_000772 18451712 NP363554.RALcltsaZPmXC_2IiDdy4YibMtFiOxpyj-4P6jmVjqBbQ130_provenance.
- NP363554.RALcltsaZPmXC_2IiDdy4YibMtFiOxpyj-4P6jmVjqBbQ130_assertion wasDerivedFrom befree-20140225 NP363554.RALcltsaZPmXC_2IiDdy4YibMtFiOxpyj-4P6jmVjqBbQ130_provenance.
- NP363554.RALcltsaZPmXC_2IiDdy4YibMtFiOxpyj-4P6jmVjqBbQ130_assertion wasGeneratedBy ECO_0000203 NP363554.RALcltsaZPmXC_2IiDdy4YibMtFiOxpyj-4P6jmVjqBbQ130_provenance.