Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP582444.RAbTC1XFHh59Iozz60-q-nXST5caPfAdNgWeyskcjvygE130_assertion> ?p ?o ?g. }
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- NP582444.RAbTC1XFHh59Iozz60-q-nXST5caPfAdNgWeyskcjvygE130_assertion type Assertion NP582444.RAbTC1XFHh59Iozz60-q-nXST5caPfAdNgWeyskcjvygE130_head.
- NP582444.RAbTC1XFHh59Iozz60-q-nXST5caPfAdNgWeyskcjvygE130_assertion wasGeneratedBy ECO_0000203 NP582444.RAbTC1XFHh59Iozz60-q-nXST5caPfAdNgWeyskcjvygE130_provenance.
- NP582444.RAbTC1XFHh59Iozz60-q-nXST5caPfAdNgWeyskcjvygE130_assertion wasDerivedFrom befree-2016 NP582444.RAbTC1XFHh59Iozz60-q-nXST5caPfAdNgWeyskcjvygE130_provenance.
- NP582444.RAbTC1XFHh59Iozz60-q-nXST5caPfAdNgWeyskcjvygE130_assertion SIO_000772 17145494 NP582444.RAbTC1XFHh59Iozz60-q-nXST5caPfAdNgWeyskcjvygE130_provenance.
- NP582444.RAbTC1XFHh59Iozz60-q-nXST5caPfAdNgWeyskcjvygE130_assertion evidence source_evidence_literature NP582444.RAbTC1XFHh59Iozz60-q-nXST5caPfAdNgWeyskcjvygE130_provenance.
- NP582444.RAbTC1XFHh59Iozz60-q-nXST5caPfAdNgWeyskcjvygE130_assertion description "[Together with earlier work implicating a distinct class of functional mutations in SCN9A in a distinct inherited pain syndrome, these results point to Na(V)1.7 channels as key players in signaling nociceptive information and as a potential target for drug therapy of chronic pain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582444.RAbTC1XFHh59Iozz60-q-nXST5caPfAdNgWeyskcjvygE130_provenance.