Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP787073.RASzh03tqVLi9aHEMgRVWR2zLFtLvOtpnG4vntKX47SIs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP787073.RASzh03tqVLi9aHEMgRVWR2zLFtLvOtpnG4vntKX47SIs130_assertion type Assertion NP787073.RASzh03tqVLi9aHEMgRVWR2zLFtLvOtpnG4vntKX47SIs130_head.
- NP787073.RASzh03tqVLi9aHEMgRVWR2zLFtLvOtpnG4vntKX47SIs130_assertion wasGeneratedBy ECO_0000203 NP787073.RASzh03tqVLi9aHEMgRVWR2zLFtLvOtpnG4vntKX47SIs130_provenance.
- NP787073.RASzh03tqVLi9aHEMgRVWR2zLFtLvOtpnG4vntKX47SIs130_assertion wasDerivedFrom befree-2016 NP787073.RASzh03tqVLi9aHEMgRVWR2zLFtLvOtpnG4vntKX47SIs130_provenance.
- NP787073.RASzh03tqVLi9aHEMgRVWR2zLFtLvOtpnG4vntKX47SIs130_assertion SIO_000772 20074229 NP787073.RASzh03tqVLi9aHEMgRVWR2zLFtLvOtpnG4vntKX47SIs130_provenance.
- NP787073.RASzh03tqVLi9aHEMgRVWR2zLFtLvOtpnG4vntKX47SIs130_assertion evidence source_evidence_literature NP787073.RASzh03tqVLi9aHEMgRVWR2zLFtLvOtpnG4vntKX47SIs130_provenance.
- NP787073.RASzh03tqVLi9aHEMgRVWR2zLFtLvOtpnG4vntKX47SIs130_assertion description "[Mutations in the voltage-gated Na(V)1.7 Na(+) channel alpha1 gene SCN9A have been linked to pain disorders, such as inherited primary erythromelalgia and paroxysmal extreme pain disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787073.RASzh03tqVLi9aHEMgRVWR2zLFtLvOtpnG4vntKX47SIs130_provenance.