Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP302200.RAdy9J0EbI7aPgloffPt3NhUkrSkbcf8NOZChMwG3UiO4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP302200.RAdy9J0EbI7aPgloffPt3NhUkrSkbcf8NOZChMwG3UiO4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP302200.RAdy9J0EbI7aPgloffPt3NhUkrSkbcf8NOZChMwG3UiO4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP302200.RAdy9J0EbI7aPgloffPt3NhUkrSkbcf8NOZChMwG3UiO4130_provenance.
- NP302200.RAdy9J0EbI7aPgloffPt3NhUkrSkbcf8NOZChMwG3UiO4130_assertion description "[Although the complex formation with hDAT occurs through the NAC domain of the alpha-synuclein variants, it is the familial Parkinson's disease-linked missense mutations present in the amino-terminal lipid binding domain of the alpha-synuclein variants that dictate the extent of the regulation of hDAT function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP302200.RAdy9J0EbI7aPgloffPt3NhUkrSkbcf8NOZChMwG3UiO4130_provenance.
- NP302200.RAdy9J0EbI7aPgloffPt3NhUkrSkbcf8NOZChMwG3UiO4130_assertion evidence source_evidence_literature NP302200.RAdy9J0EbI7aPgloffPt3NhUkrSkbcf8NOZChMwG3UiO4130_provenance.
- NP302200.RAdy9J0EbI7aPgloffPt3NhUkrSkbcf8NOZChMwG3UiO4130_assertion SIO_000772 14550771 NP302200.RAdy9J0EbI7aPgloffPt3NhUkrSkbcf8NOZChMwG3UiO4130_provenance.
- NP302200.RAdy9J0EbI7aPgloffPt3NhUkrSkbcf8NOZChMwG3UiO4130_assertion wasDerivedFrom befree-20140225 NP302200.RAdy9J0EbI7aPgloffPt3NhUkrSkbcf8NOZChMwG3UiO4130_provenance.
- NP302200.RAdy9J0EbI7aPgloffPt3NhUkrSkbcf8NOZChMwG3UiO4130_assertion wasGeneratedBy ECO_0000203 NP302200.RAdy9J0EbI7aPgloffPt3NhUkrSkbcf8NOZChMwG3UiO4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP302200.RAdy9J0EbI7aPgloffPt3NhUkrSkbcf8NOZChMwG3UiO4130_provenance.