Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1259515.RA5vROz-lNDgLHu1rFAJ_AFnXhgQdowen6twz234UcGjE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1259515.RA5vROz-lNDgLHu1rFAJ_AFnXhgQdowen6twz234UcGjE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1259515.RA5vROz-lNDgLHu1rFAJ_AFnXhgQdowen6twz234UcGjE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1259515.RA5vROz-lNDgLHu1rFAJ_AFnXhgQdowen6twz234UcGjE130_provenance.
- NP1259515.RA5vROz-lNDgLHu1rFAJ_AFnXhgQdowen6twz234UcGjE130_assertion description "[We propose that this GCH1 variant is pathogenic in this family and these findings suggest that similar mechanisms involving abnormal GTP cyclohydolase I may underlie both PD and DRD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1259515.RA5vROz-lNDgLHu1rFAJ_AFnXhgQdowen6twz234UcGjE130_provenance.
- NP1259515.RA5vROz-lNDgLHu1rFAJ_AFnXhgQdowen6twz234UcGjE130_assertion evidence source_evidence_literature NP1259515.RA5vROz-lNDgLHu1rFAJ_AFnXhgQdowen6twz234UcGjE130_provenance.
- NP1259515.RA5vROz-lNDgLHu1rFAJ_AFnXhgQdowen6twz234UcGjE130_assertion SIO_000772 25634433 NP1259515.RA5vROz-lNDgLHu1rFAJ_AFnXhgQdowen6twz234UcGjE130_provenance.
- NP1259515.RA5vROz-lNDgLHu1rFAJ_AFnXhgQdowen6twz234UcGjE130_assertion wasDerivedFrom befree-2016 NP1259515.RA5vROz-lNDgLHu1rFAJ_AFnXhgQdowen6twz234UcGjE130_provenance.
- NP1259515.RA5vROz-lNDgLHu1rFAJ_AFnXhgQdowen6twz234UcGjE130_assertion wasGeneratedBy ECO_0000203 NP1259515.RA5vROz-lNDgLHu1rFAJ_AFnXhgQdowen6twz234UcGjE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1259515.RA5vROz-lNDgLHu1rFAJ_AFnXhgQdowen6twz234UcGjE130_provenance.