Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP362818.RA5jTyXvtBc3HgsdmPfZFSFploUJ3ONVOBt4_Ilx3HhQU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP362818.RA5jTyXvtBc3HgsdmPfZFSFploUJ3ONVOBt4_Ilx3HhQU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP362818.RA5jTyXvtBc3HgsdmPfZFSFploUJ3ONVOBt4_Ilx3HhQU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP362818.RA5jTyXvtBc3HgsdmPfZFSFploUJ3ONVOBt4_Ilx3HhQU130_provenance.
- NP362818.RA5jTyXvtBc3HgsdmPfZFSFploUJ3ONVOBt4_Ilx3HhQU130_assertion description "[DYT1 primary torsion dystonia is an autosomal dominant movement disorder due to a 3-bp GAG deletion in the TOR1A gene, which becomes manifest in only 30-40% of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362818.RA5jTyXvtBc3HgsdmPfZFSFploUJ3ONVOBt4_Ilx3HhQU130_provenance.
- NP362818.RA5jTyXvtBc3HgsdmPfZFSFploUJ3ONVOBt4_Ilx3HhQU130_assertion evidence source_evidence_literature NP362818.RA5jTyXvtBc3HgsdmPfZFSFploUJ3ONVOBt4_Ilx3HhQU130_provenance.
- NP362818.RA5jTyXvtBc3HgsdmPfZFSFploUJ3ONVOBt4_Ilx3HhQU130_assertion SIO_000772 17105745 NP362818.RA5jTyXvtBc3HgsdmPfZFSFploUJ3ONVOBt4_Ilx3HhQU130_provenance.
- NP362818.RA5jTyXvtBc3HgsdmPfZFSFploUJ3ONVOBt4_Ilx3HhQU130_assertion wasDerivedFrom befree-20150227 NP362818.RA5jTyXvtBc3HgsdmPfZFSFploUJ3ONVOBt4_Ilx3HhQU130_provenance.
- NP362818.RA5jTyXvtBc3HgsdmPfZFSFploUJ3ONVOBt4_Ilx3HhQU130_assertion wasGeneratedBy ECO_0000203 NP362818.RA5jTyXvtBc3HgsdmPfZFSFploUJ3ONVOBt4_Ilx3HhQU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP362818.RA5jTyXvtBc3HgsdmPfZFSFploUJ3ONVOBt4_Ilx3HhQU130_provenance.