Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP370509.RAkm0frX1skAGfzPajjZRB5pkIkJMGvLjVHs_E-9PAGCQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP370509.RAkm0frX1skAGfzPajjZRB5pkIkJMGvLjVHs_E-9PAGCQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP370509.RAkm0frX1skAGfzPajjZRB5pkIkJMGvLjVHs_E-9PAGCQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP370509.RAkm0frX1skAGfzPajjZRB5pkIkJMGvLjVHs_E-9PAGCQ130_provenance.
- NP370509.RAkm0frX1skAGfzPajjZRB5pkIkJMGvLjVHs_E-9PAGCQ130_assertion description "[We found that mutations of GTP cyclohydrolase I, the rate-limiting enzyme in the biosynthesis of tetrahydrobiopterin, which is the cofactor of dopamine-synthesizing tyrosine hydroxylase, cause dominantly inherited hereditary progressive dystonia with marked diurnal fluctuation (HPD, Segawa's disease) probably owing to the decrease of dopamine in the basal ganglia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP370509.RAkm0frX1skAGfzPajjZRB5pkIkJMGvLjVHs_E-9PAGCQ130_provenance.
- NP370509.RAkm0frX1skAGfzPajjZRB5pkIkJMGvLjVHs_E-9PAGCQ130_assertion evidence source_evidence_literature NP370509.RAkm0frX1skAGfzPajjZRB5pkIkJMGvLjVHs_E-9PAGCQ130_provenance.
- NP370509.RAkm0frX1skAGfzPajjZRB5pkIkJMGvLjVHs_E-9PAGCQ130_assertion SIO_000772 9205791 NP370509.RAkm0frX1skAGfzPajjZRB5pkIkJMGvLjVHs_E-9PAGCQ130_provenance.
- NP370509.RAkm0frX1skAGfzPajjZRB5pkIkJMGvLjVHs_E-9PAGCQ130_assertion wasDerivedFrom befree-20140225 NP370509.RAkm0frX1skAGfzPajjZRB5pkIkJMGvLjVHs_E-9PAGCQ130_provenance.
- NP370509.RAkm0frX1skAGfzPajjZRB5pkIkJMGvLjVHs_E-9PAGCQ130_assertion wasGeneratedBy ECO_0000203 NP370509.RAkm0frX1skAGfzPajjZRB5pkIkJMGvLjVHs_E-9PAGCQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP370509.RAkm0frX1skAGfzPajjZRB5pkIkJMGvLjVHs_E-9PAGCQ130_provenance.