Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP669013.RAvFNkWWLTRkgvqB1oeUx2HupTJdlfoCjtDv-GFoawdNw130_assertion> ?p ?o ?g. }
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- NP669013.RAvFNkWWLTRkgvqB1oeUx2HupTJdlfoCjtDv-GFoawdNw130_assertion type Assertion NP669013.RAvFNkWWLTRkgvqB1oeUx2HupTJdlfoCjtDv-GFoawdNw130_head.
- NP669013.RAvFNkWWLTRkgvqB1oeUx2HupTJdlfoCjtDv-GFoawdNw130_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." NP669013.RAvFNkWWLTRkgvqB1oeUx2HupTJdlfoCjtDv-GFoawdNw130_provenance.
- NP669013.RAvFNkWWLTRkgvqB1oeUx2HupTJdlfoCjtDv-GFoawdNw130_assertion evidence source_evidence_literature NP669013.RAvFNkWWLTRkgvqB1oeUx2HupTJdlfoCjtDv-GFoawdNw130_provenance.
- NP669013.RAvFNkWWLTRkgvqB1oeUx2HupTJdlfoCjtDv-GFoawdNw130_assertion SIO_000772 18451712 NP669013.RAvFNkWWLTRkgvqB1oeUx2HupTJdlfoCjtDv-GFoawdNw130_provenance.
- NP669013.RAvFNkWWLTRkgvqB1oeUx2HupTJdlfoCjtDv-GFoawdNw130_assertion wasDerivedFrom befree-2016 NP669013.RAvFNkWWLTRkgvqB1oeUx2HupTJdlfoCjtDv-GFoawdNw130_provenance.
- NP669013.RAvFNkWWLTRkgvqB1oeUx2HupTJdlfoCjtDv-GFoawdNw130_assertion wasGeneratedBy ECO_0000203 NP669013.RAvFNkWWLTRkgvqB1oeUx2HupTJdlfoCjtDv-GFoawdNw130_provenance.