Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP811002.RA7nhaRjJeyvIc8AYgncFG3hqmgz1qQK06mvXQ4VbMKMs130_assertion> ?p ?o ?g. }
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- NP811002.RA7nhaRjJeyvIc8AYgncFG3hqmgz1qQK06mvXQ4VbMKMs130_assertion type Assertion NP811002.RA7nhaRjJeyvIc8AYgncFG3hqmgz1qQK06mvXQ4VbMKMs130_head.
- NP811002.RA7nhaRjJeyvIc8AYgncFG3hqmgz1qQK06mvXQ4VbMKMs130_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." NP811002.RA7nhaRjJeyvIc8AYgncFG3hqmgz1qQK06mvXQ4VbMKMs130_provenance.
- NP811002.RA7nhaRjJeyvIc8AYgncFG3hqmgz1qQK06mvXQ4VbMKMs130_assertion evidence source_evidence_literature NP811002.RA7nhaRjJeyvIc8AYgncFG3hqmgz1qQK06mvXQ4VbMKMs130_provenance.
- NP811002.RA7nhaRjJeyvIc8AYgncFG3hqmgz1qQK06mvXQ4VbMKMs130_assertion SIO_000772 22515636 NP811002.RA7nhaRjJeyvIc8AYgncFG3hqmgz1qQK06mvXQ4VbMKMs130_provenance.
- NP811002.RA7nhaRjJeyvIc8AYgncFG3hqmgz1qQK06mvXQ4VbMKMs130_assertion wasDerivedFrom befree-20150227 NP811002.RA7nhaRjJeyvIc8AYgncFG3hqmgz1qQK06mvXQ4VbMKMs130_provenance.
- NP811002.RA7nhaRjJeyvIc8AYgncFG3hqmgz1qQK06mvXQ4VbMKMs130_assertion wasGeneratedBy ECO_0000203 NP811002.RA7nhaRjJeyvIc8AYgncFG3hqmgz1qQK06mvXQ4VbMKMs130_provenance.