Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP256104.RASOa3rQXsQvz-j2oUYfZ9Z8g9Ig1oyYpe_CkNhOA6CsA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP256104.RASOa3rQXsQvz-j2oUYfZ9Z8g9Ig1oyYpe_CkNhOA6CsA130_assertion type Assertion NP256104.RASOa3rQXsQvz-j2oUYfZ9Z8g9Ig1oyYpe_CkNhOA6CsA130_head.
- NP256104.RASOa3rQXsQvz-j2oUYfZ9Z8g9Ig1oyYpe_CkNhOA6CsA130_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." NP256104.RASOa3rQXsQvz-j2oUYfZ9Z8g9Ig1oyYpe_CkNhOA6CsA130_provenance.
- NP256104.RASOa3rQXsQvz-j2oUYfZ9Z8g9Ig1oyYpe_CkNhOA6CsA130_assertion evidence source_evidence_literature NP256104.RASOa3rQXsQvz-j2oUYfZ9Z8g9Ig1oyYpe_CkNhOA6CsA130_provenance.
- NP256104.RASOa3rQXsQvz-j2oUYfZ9Z8g9Ig1oyYpe_CkNhOA6CsA130_assertion SIO_000772 18451712 NP256104.RASOa3rQXsQvz-j2oUYfZ9Z8g9Ig1oyYpe_CkNhOA6CsA130_provenance.
- NP256104.RASOa3rQXsQvz-j2oUYfZ9Z8g9Ig1oyYpe_CkNhOA6CsA130_assertion wasDerivedFrom befree-20150227 NP256104.RASOa3rQXsQvz-j2oUYfZ9Z8g9Ig1oyYpe_CkNhOA6CsA130_provenance.
- NP256104.RASOa3rQXsQvz-j2oUYfZ9Z8g9Ig1oyYpe_CkNhOA6CsA130_assertion wasGeneratedBy ECO_0000203 NP256104.RASOa3rQXsQvz-j2oUYfZ9Z8g9Ig1oyYpe_CkNhOA6CsA130_provenance.