Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_assertion> ?p ?o ?g. }
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- NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_assertion type Assertion NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_head.
- NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_assertion description "[Rapid-onset dystonia-parkinsonism (RDP, DYT12) is a distinctive autosomal-dominant movement disorder with variable expressivity and reduced penetrance characterized by abrupt onset of dystonia, usually accompanied by signs of parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_provenance.
- NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_assertion evidence source_evidence_curated NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_provenance.
- NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_assertion SIO_000772 15260953 NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_provenance.
- NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_assertion wasDerivedFrom ctd_human-20150221 NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_provenance.
- NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_assertion wasGeneratedBy ECO_0000218 NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_provenance.