Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_provenance.
- 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.
- ctd_human-20150221 importedOn "2015-02-21" NP7695.RAMBFs9JG1tX0Zud8hTmAUmW9MCzZbPI9oDss6EMNq7w8130_provenance.