Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP613675.RACnQH2chHBu4r-tbYToMTS4Ym2losy_0NAteVUbR-Hp4130_assertion> ?p ?o ?g. }
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- NP613675.RACnQH2chHBu4r-tbYToMTS4Ym2losy_0NAteVUbR-Hp4130_assertion type Assertion NP613675.RACnQH2chHBu4r-tbYToMTS4Ym2losy_0NAteVUbR-Hp4130_head.
- NP613675.RACnQH2chHBu4r-tbYToMTS4Ym2losy_0NAteVUbR-Hp4130_assertion description "[Four patients had a deletion of a known movement disorder gene including paroxysmal kinesigenic dyskinesia (PRRT2; n=2), SGCE (myoclonus dystonia, n=1), and TITF1 (benign hereditary chorea, n=1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP613675.RACnQH2chHBu4r-tbYToMTS4Ym2losy_0NAteVUbR-Hp4130_provenance.
- NP613675.RACnQH2chHBu4r-tbYToMTS4Ym2losy_0NAteVUbR-Hp4130_assertion evidence source_evidence_literature NP613675.RACnQH2chHBu4r-tbYToMTS4Ym2losy_0NAteVUbR-Hp4130_provenance.
- NP613675.RACnQH2chHBu4r-tbYToMTS4Ym2losy_0NAteVUbR-Hp4130_assertion SIO_000772 22515636 NP613675.RACnQH2chHBu4r-tbYToMTS4Ym2losy_0NAteVUbR-Hp4130_provenance.
- NP613675.RACnQH2chHBu4r-tbYToMTS4Ym2losy_0NAteVUbR-Hp4130_assertion wasDerivedFrom befree-20140225 NP613675.RACnQH2chHBu4r-tbYToMTS4Ym2losy_0NAteVUbR-Hp4130_provenance.
- NP613675.RACnQH2chHBu4r-tbYToMTS4Ym2losy_0NAteVUbR-Hp4130_assertion wasGeneratedBy ECO_0000203 NP613675.RACnQH2chHBu4r-tbYToMTS4Ym2losy_0NAteVUbR-Hp4130_provenance.