Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP683459.RAddQ7vuMXvIxcBhV1nYLEWxU4wtKGH28rvPgLpoZNHpw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP683459.RAddQ7vuMXvIxcBhV1nYLEWxU4wtKGH28rvPgLpoZNHpw130_assertion type Assertion NP683459.RAddQ7vuMXvIxcBhV1nYLEWxU4wtKGH28rvPgLpoZNHpw130_head.
- NP683459.RAddQ7vuMXvIxcBhV1nYLEWxU4wtKGH28rvPgLpoZNHpw130_assertion wasGeneratedBy ECO_0000203 NP683459.RAddQ7vuMXvIxcBhV1nYLEWxU4wtKGH28rvPgLpoZNHpw130_provenance.
- NP683459.RAddQ7vuMXvIxcBhV1nYLEWxU4wtKGH28rvPgLpoZNHpw130_assertion wasDerivedFrom befree-20150227 NP683459.RAddQ7vuMXvIxcBhV1nYLEWxU4wtKGH28rvPgLpoZNHpw130_provenance.
- NP683459.RAddQ7vuMXvIxcBhV1nYLEWxU4wtKGH28rvPgLpoZNHpw130_assertion SIO_000772 17145494 NP683459.RAddQ7vuMXvIxcBhV1nYLEWxU4wtKGH28rvPgLpoZNHpw130_provenance.
- NP683459.RAddQ7vuMXvIxcBhV1nYLEWxU4wtKGH28rvPgLpoZNHpw130_assertion evidence source_evidence_literature NP683459.RAddQ7vuMXvIxcBhV1nYLEWxU4wtKGH28rvPgLpoZNHpw130_provenance.
- NP683459.RAddQ7vuMXvIxcBhV1nYLEWxU4wtKGH28rvPgLpoZNHpw130_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." NP683459.RAddQ7vuMXvIxcBhV1nYLEWxU4wtKGH28rvPgLpoZNHpw130_provenance.