Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP695854.RA0RwI_K2dY03jjcV_G61j2a1NEnB81CUghto_pyOiHBQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP695854.RA0RwI_K2dY03jjcV_G61j2a1NEnB81CUghto_pyOiHBQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP695854.RA0RwI_K2dY03jjcV_G61j2a1NEnB81CUghto_pyOiHBQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP695854.RA0RwI_K2dY03jjcV_G61j2a1NEnB81CUghto_pyOiHBQ130_provenance.
- NP695854.RA0RwI_K2dY03jjcV_G61j2a1NEnB81CUghto_pyOiHBQ130_assertion description "[Finally, paroxysmal exertion-induced dystonia (DYT18, GLUT1 deficiency) is caused by mutations in the SLC2A1 gene (DYT9 and DYT18).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695854.RA0RwI_K2dY03jjcV_G61j2a1NEnB81CUghto_pyOiHBQ130_provenance.
- NP695854.RA0RwI_K2dY03jjcV_G61j2a1NEnB81CUghto_pyOiHBQ130_assertion evidence source_evidence_literature NP695854.RA0RwI_K2dY03jjcV_G61j2a1NEnB81CUghto_pyOiHBQ130_provenance.
- NP695854.RA0RwI_K2dY03jjcV_G61j2a1NEnB81CUghto_pyOiHBQ130_assertion SIO_000772 22166420 NP695854.RA0RwI_K2dY03jjcV_G61j2a1NEnB81CUghto_pyOiHBQ130_provenance.
- NP695854.RA0RwI_K2dY03jjcV_G61j2a1NEnB81CUghto_pyOiHBQ130_assertion wasDerivedFrom befree-20150227 NP695854.RA0RwI_K2dY03jjcV_G61j2a1NEnB81CUghto_pyOiHBQ130_provenance.
- NP695854.RA0RwI_K2dY03jjcV_G61j2a1NEnB81CUghto_pyOiHBQ130_assertion wasGeneratedBy ECO_0000203 NP695854.RA0RwI_K2dY03jjcV_G61j2a1NEnB81CUghto_pyOiHBQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP695854.RA0RwI_K2dY03jjcV_G61j2a1NEnB81CUghto_pyOiHBQ130_provenance.