Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP87772.RAbm4yDvL7h2QF8H2JZawc-bLMw72Le9WS4ncs1mfP14c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP87772.RAbm4yDvL7h2QF8H2JZawc-bLMw72Le9WS4ncs1mfP14c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP87772.RAbm4yDvL7h2QF8H2JZawc-bLMw72Le9WS4ncs1mfP14c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP87772.RAbm4yDvL7h2QF8H2JZawc-bLMw72Le9WS4ncs1mfP14c130_provenance.
- NP87772.RAbm4yDvL7h2QF8H2JZawc-bLMw72Le9WS4ncs1mfP14c130_assertion description "[ The results of the study suggest that patients with COMT(L/L) genotype and possibly MAOB genotype A may benefit from more efficient and safer levodopa therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87772.RAbm4yDvL7h2QF8H2JZawc-bLMw72Le9WS4ncs1mfP14c130_provenance.
- NP87772.RAbm4yDvL7h2QF8H2JZawc-bLMw72Le9WS4ncs1mfP14c130_assertion evidence source_evidence_literature NP87772.RAbm4yDvL7h2QF8H2JZawc-bLMw72Le9WS4ncs1mfP14c130_provenance.
- NP87772.RAbm4yDvL7h2QF8H2JZawc-bLMw72Le9WS4ncs1mfP14c130_assertion SIO_000772 15355491 NP87772.RAbm4yDvL7h2QF8H2JZawc-bLMw72Le9WS4ncs1mfP14c130_provenance.
- NP87772.RAbm4yDvL7h2QF8H2JZawc-bLMw72Le9WS4ncs1mfP14c130_assertion wasDerivedFrom gad-20150221 NP87772.RAbm4yDvL7h2QF8H2JZawc-bLMw72Le9WS4ncs1mfP14c130_provenance.
- NP87772.RAbm4yDvL7h2QF8H2JZawc-bLMw72Le9WS4ncs1mfP14c130_assertion wasGeneratedBy ECO_0000203 NP87772.RAbm4yDvL7h2QF8H2JZawc-bLMw72Le9WS4ncs1mfP14c130_provenance.
- gad-20150221 importedOn "2015-02-21" NP87772.RAbm4yDvL7h2QF8H2JZawc-bLMw72Le9WS4ncs1mfP14c130_provenance.