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- source_evidence_literature type ECO_0000212 NP1259518.RApe523k0dOARGRw6ALxGeJAPu6haIUxHggSGTNkPD-ng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1259518.RApe523k0dOARGRw6ALxGeJAPu6haIUxHggSGTNkPD-ng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1259518.RApe523k0dOARGRw6ALxGeJAPu6haIUxHggSGTNkPD-ng130_provenance.
- NP1259518.RApe523k0dOARGRw6ALxGeJAPu6haIUxHggSGTNkPD-ng130_assertion description "[These two with abnormal DAT imaging had a PD phenotype, while the remaining three subjects with the novel GCH1 variant had normal DAT imaging and a DRD phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1259518.RApe523k0dOARGRw6ALxGeJAPu6haIUxHggSGTNkPD-ng130_provenance.
- NP1259518.RApe523k0dOARGRw6ALxGeJAPu6haIUxHggSGTNkPD-ng130_assertion evidence source_evidence_literature NP1259518.RApe523k0dOARGRw6ALxGeJAPu6haIUxHggSGTNkPD-ng130_provenance.
- NP1259518.RApe523k0dOARGRw6ALxGeJAPu6haIUxHggSGTNkPD-ng130_assertion SIO_000772 25634433 NP1259518.RApe523k0dOARGRw6ALxGeJAPu6haIUxHggSGTNkPD-ng130_provenance.
- NP1259518.RApe523k0dOARGRw6ALxGeJAPu6haIUxHggSGTNkPD-ng130_assertion wasDerivedFrom befree-2016 NP1259518.RApe523k0dOARGRw6ALxGeJAPu6haIUxHggSGTNkPD-ng130_provenance.
- NP1259518.RApe523k0dOARGRw6ALxGeJAPu6haIUxHggSGTNkPD-ng130_assertion wasGeneratedBy ECO_0000203 NP1259518.RApe523k0dOARGRw6ALxGeJAPu6haIUxHggSGTNkPD-ng130_provenance.
- befree-2016 importedOn "2016-02-19" NP1259518.RApe523k0dOARGRw6ALxGeJAPu6haIUxHggSGTNkPD-ng130_provenance.