Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_provenance.
- NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_assertion description "[All the subjects except for one family had typical manifestations of autosomal dominant GTPCH-I deficient DRD including early childhood onset dystonia predominantly in the legs, marked diurnal variation, intact cognition, no other systemic symptoms, and excellent sustained response to levodopa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_provenance.
- NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_assertion evidence source_evidence_literature NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_provenance.
- NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_assertion SIO_000772 24018121 NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_provenance.
- NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_assertion wasDerivedFrom befree-2016 NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_provenance.
- NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_assertion wasGeneratedBy ECO_0000203 NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_provenance.
- befree-2016 importedOn "2016-02-19" NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_provenance.