Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP928962.RAXzAIipZTaQMjb-nWfnMsKA6hXssw5VvU0oD8ezHWzCw130_assertion> ?p ?o ?g. }
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- NP928962.RAXzAIipZTaQMjb-nWfnMsKA6hXssw5VvU0oD8ezHWzCw130_assertion type Assertion NP928962.RAXzAIipZTaQMjb-nWfnMsKA6hXssw5VvU0oD8ezHWzCw130_head.
- NP928962.RAXzAIipZTaQMjb-nWfnMsKA6hXssw5VvU0oD8ezHWzCw130_assertion description "[We screened 230 individuals with primary periodic paralysis for mutations in the SCN4A, CACNA1S, and KCNJ2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP928962.RAXzAIipZTaQMjb-nWfnMsKA6hXssw5VvU0oD8ezHWzCw130_provenance.
- NP928962.RAXzAIipZTaQMjb-nWfnMsKA6hXssw5VvU0oD8ezHWzCw130_assertion evidence source_evidence_literature NP928962.RAXzAIipZTaQMjb-nWfnMsKA6hXssw5VvU0oD8ezHWzCw130_provenance.
- NP928962.RAXzAIipZTaQMjb-nWfnMsKA6hXssw5VvU0oD8ezHWzCw130_assertion SIO_000772 22926674 NP928962.RAXzAIipZTaQMjb-nWfnMsKA6hXssw5VvU0oD8ezHWzCw130_provenance.
- NP928962.RAXzAIipZTaQMjb-nWfnMsKA6hXssw5VvU0oD8ezHWzCw130_assertion wasDerivedFrom befree-20140225 NP928962.RAXzAIipZTaQMjb-nWfnMsKA6hXssw5VvU0oD8ezHWzCw130_provenance.
- NP928962.RAXzAIipZTaQMjb-nWfnMsKA6hXssw5VvU0oD8ezHWzCw130_assertion wasGeneratedBy ECO_0000203 NP928962.RAXzAIipZTaQMjb-nWfnMsKA6hXssw5VvU0oD8ezHWzCw130_provenance.