Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_provenance.
- NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_provenance.
- NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_assertion evidence source_evidence_literature NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_provenance.
- NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_assertion SIO_000772 19578124 NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_provenance.
- NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_assertion wasDerivedFrom befree-20150227 NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_provenance.
- NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_assertion wasGeneratedBy ECO_0000203 NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_provenance.