Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP142207.RAJJW1r1_GhMEfXkgh-z7ReurN1og8bQ7uYr82RFbRmms130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP142207.RAJJW1r1_GhMEfXkgh-z7ReurN1og8bQ7uYr82RFbRmms130_assertion type Assertion NP142207.RAJJW1r1_GhMEfXkgh-z7ReurN1og8bQ7uYr82RFbRmms130_head.
- NP142207.RAJJW1r1_GhMEfXkgh-z7ReurN1og8bQ7uYr82RFbRmms130_assertion wasGeneratedBy ECO_0000203 NP142207.RAJJW1r1_GhMEfXkgh-z7ReurN1og8bQ7uYr82RFbRmms130_provenance.
- NP142207.RAJJW1r1_GhMEfXkgh-z7ReurN1og8bQ7uYr82RFbRmms130_assertion wasDerivedFrom lhgdn-20090331 NP142207.RAJJW1r1_GhMEfXkgh-z7ReurN1og8bQ7uYr82RFbRmms130_provenance.
- NP142207.RAJJW1r1_GhMEfXkgh-z7ReurN1og8bQ7uYr82RFbRmms130_assertion SIO_000772 18021921 NP142207.RAJJW1r1_GhMEfXkgh-z7ReurN1og8bQ7uYr82RFbRmms130_provenance.
- NP142207.RAJJW1r1_GhMEfXkgh-z7ReurN1og8bQ7uYr82RFbRmms130_assertion evidence source_evidence_literature NP142207.RAJJW1r1_GhMEfXkgh-z7ReurN1og8bQ7uYr82RFbRmms130_provenance.
- NP142207.RAJJW1r1_GhMEfXkgh-z7ReurN1og8bQ7uYr82RFbRmms130_assertion description "[The novel T1174S missense mutation of SCN1A gene was detected segregating in a family with a heterozygous female child and in her heterozygous mother, who had an ataxic migraine syndrome similar to that of her own mother.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP142207.RAJJW1r1_GhMEfXkgh-z7ReurN1og8bQ7uYr82RFbRmms130_provenance.