Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1051802.RA80wTqv0odw79P8Cnr1CPx4HDp2oXaLmz0Cv0XqiUylc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1051802.RA80wTqv0odw79P8Cnr1CPx4HDp2oXaLmz0Cv0XqiUylc130_assertion type Assertion NP1051802.RA80wTqv0odw79P8Cnr1CPx4HDp2oXaLmz0Cv0XqiUylc130_head.
- NP1051802.RA80wTqv0odw79P8Cnr1CPx4HDp2oXaLmz0Cv0XqiUylc130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1051802.RA80wTqv0odw79P8Cnr1CPx4HDp2oXaLmz0Cv0XqiUylc130_provenance.
- NP1051802.RA80wTqv0odw79P8Cnr1CPx4HDp2oXaLmz0Cv0XqiUylc130_assertion evidence source_evidence_literature NP1051802.RA80wTqv0odw79P8Cnr1CPx4HDp2oXaLmz0Cv0XqiUylc130_provenance.
- NP1051802.RA80wTqv0odw79P8Cnr1CPx4HDp2oXaLmz0Cv0XqiUylc130_assertion SIO_000772 23398397 NP1051802.RA80wTqv0odw79P8Cnr1CPx4HDp2oXaLmz0Cv0XqiUylc130_provenance.
- NP1051802.RA80wTqv0odw79P8Cnr1CPx4HDp2oXaLmz0Cv0XqiUylc130_assertion wasDerivedFrom befree-2016 NP1051802.RA80wTqv0odw79P8Cnr1CPx4HDp2oXaLmz0Cv0XqiUylc130_provenance.
- NP1051802.RA80wTqv0odw79P8Cnr1CPx4HDp2oXaLmz0Cv0XqiUylc130_assertion wasGeneratedBy ECO_0000203 NP1051802.RA80wTqv0odw79P8Cnr1CPx4HDp2oXaLmz0Cv0XqiUylc130_provenance.