Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP67854.RAeSoRaKGykkZQDv1pl6DcOEkWVlwkLIl8hvhdy1aJNF8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP67854.RAeSoRaKGykkZQDv1pl6DcOEkWVlwkLIl8hvhdy1aJNF8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP67854.RAeSoRaKGykkZQDv1pl6DcOEkWVlwkLIl8hvhdy1aJNF8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP67854.RAeSoRaKGykkZQDv1pl6DcOEkWVlwkLIl8hvhdy1aJNF8130_provenance.
- NP67854.RAeSoRaKGykkZQDv1pl6DcOEkWVlwkLIl8hvhdy1aJNF8130_assertion description "[Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP67854.RAeSoRaKGykkZQDv1pl6DcOEkWVlwkLIl8hvhdy1aJNF8130_provenance.
- NP67854.RAeSoRaKGykkZQDv1pl6DcOEkWVlwkLIl8hvhdy1aJNF8130_assertion evidence source_evidence_literature NP67854.RAeSoRaKGykkZQDv1pl6DcOEkWVlwkLIl8hvhdy1aJNF8130_provenance.
- NP67854.RAeSoRaKGykkZQDv1pl6DcOEkWVlwkLIl8hvhdy1aJNF8130_assertion SIO_000772 10923647 NP67854.RAeSoRaKGykkZQDv1pl6DcOEkWVlwkLIl8hvhdy1aJNF8130_provenance.
- NP67854.RAeSoRaKGykkZQDv1pl6DcOEkWVlwkLIl8hvhdy1aJNF8130_assertion wasDerivedFrom gad-20150221 NP67854.RAeSoRaKGykkZQDv1pl6DcOEkWVlwkLIl8hvhdy1aJNF8130_provenance.
- NP67854.RAeSoRaKGykkZQDv1pl6DcOEkWVlwkLIl8hvhdy1aJNF8130_assertion wasGeneratedBy ECO_0000203 NP67854.RAeSoRaKGykkZQDv1pl6DcOEkWVlwkLIl8hvhdy1aJNF8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP67854.RAeSoRaKGykkZQDv1pl6DcOEkWVlwkLIl8hvhdy1aJNF8130_provenance.