Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP742635.RAaNGU4tVzGRXJlt2evAejuRH-1OP5Fumkvp_JaAfaNyc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP742635.RAaNGU4tVzGRXJlt2evAejuRH-1OP5Fumkvp_JaAfaNyc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP742635.RAaNGU4tVzGRXJlt2evAejuRH-1OP5Fumkvp_JaAfaNyc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP742635.RAaNGU4tVzGRXJlt2evAejuRH-1OP5Fumkvp_JaAfaNyc130_provenance.
- NP742635.RAaNGU4tVzGRXJlt2evAejuRH-1OP5Fumkvp_JaAfaNyc130_assertion description "[Patient with mutation in the PARK2 gene had Dopa-responsive dystonia with a good improvement with L-Dopa, similar to Dopa-responsive dystonia secondary to GCH1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP742635.RAaNGU4tVzGRXJlt2evAejuRH-1OP5Fumkvp_JaAfaNyc130_provenance.
- NP742635.RAaNGU4tVzGRXJlt2evAejuRH-1OP5Fumkvp_JaAfaNyc130_assertion evidence source_evidence_literature NP742635.RAaNGU4tVzGRXJlt2evAejuRH-1OP5Fumkvp_JaAfaNyc130_provenance.
- NP742635.RAaNGU4tVzGRXJlt2evAejuRH-1OP5Fumkvp_JaAfaNyc130_assertion SIO_000772 19491146 NP742635.RAaNGU4tVzGRXJlt2evAejuRH-1OP5Fumkvp_JaAfaNyc130_provenance.
- NP742635.RAaNGU4tVzGRXJlt2evAejuRH-1OP5Fumkvp_JaAfaNyc130_assertion wasDerivedFrom befree-2016 NP742635.RAaNGU4tVzGRXJlt2evAejuRH-1OP5Fumkvp_JaAfaNyc130_provenance.
- NP742635.RAaNGU4tVzGRXJlt2evAejuRH-1OP5Fumkvp_JaAfaNyc130_assertion wasGeneratedBy ECO_0000203 NP742635.RAaNGU4tVzGRXJlt2evAejuRH-1OP5Fumkvp_JaAfaNyc130_provenance.
- befree-2016 importedOn "2016-02-19" NP742635.RAaNGU4tVzGRXJlt2evAejuRH-1OP5Fumkvp_JaAfaNyc130_provenance.