Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP362791.RAbJyeX5PhU3Urtrqw_CIaoKNAGS8vHjiI9koXHd9hCiA130_assertion> ?p ?o ?g. }
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- NP362791.RAbJyeX5PhU3Urtrqw_CIaoKNAGS8vHjiI9koXHd9hCiA130_assertion type Assertion NP362791.RAbJyeX5PhU3Urtrqw_CIaoKNAGS8vHjiI9koXHd9hCiA130_head.
- NP362791.RAbJyeX5PhU3Urtrqw_CIaoKNAGS8vHjiI9koXHd9hCiA130_assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362791.RAbJyeX5PhU3Urtrqw_CIaoKNAGS8vHjiI9koXHd9hCiA130_provenance.
- NP362791.RAbJyeX5PhU3Urtrqw_CIaoKNAGS8vHjiI9koXHd9hCiA130_assertion evidence source_evidence_literature NP362791.RAbJyeX5PhU3Urtrqw_CIaoKNAGS8vHjiI9koXHd9hCiA130_provenance.
- NP362791.RAbJyeX5PhU3Urtrqw_CIaoKNAGS8vHjiI9koXHd9hCiA130_assertion SIO_000772 23911094 NP362791.RAbJyeX5PhU3Urtrqw_CIaoKNAGS8vHjiI9koXHd9hCiA130_provenance.
- NP362791.RAbJyeX5PhU3Urtrqw_CIaoKNAGS8vHjiI9koXHd9hCiA130_assertion wasDerivedFrom befree-20150227 NP362791.RAbJyeX5PhU3Urtrqw_CIaoKNAGS8vHjiI9koXHd9hCiA130_provenance.
- NP362791.RAbJyeX5PhU3Urtrqw_CIaoKNAGS8vHjiI9koXHd9hCiA130_assertion wasGeneratedBy ECO_0000203 NP362791.RAbJyeX5PhU3Urtrqw_CIaoKNAGS8vHjiI9koXHd9hCiA130_provenance.