Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP698487.RAv2pE1TUrcNn1wdQRvYyEvL0XjGpZyuFv3U9WHpIK8_Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP698487.RAv2pE1TUrcNn1wdQRvYyEvL0XjGpZyuFv3U9WHpIK8_Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP698487.RAv2pE1TUrcNn1wdQRvYyEvL0XjGpZyuFv3U9WHpIK8_Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP698487.RAv2pE1TUrcNn1wdQRvYyEvL0XjGpZyuFv3U9WHpIK8_Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP698487.RAv2pE1TUrcNn1wdQRvYyEvL0XjGpZyuFv3U9WHpIK8_Y130_provenance.
- NP698487.RAv2pE1TUrcNn1wdQRvYyEvL0XjGpZyuFv3U9WHpIK8_Y130_assertion wasGeneratedBy ECO_0000203 NP698487.RAv2pE1TUrcNn1wdQRvYyEvL0XjGpZyuFv3U9WHpIK8_Y130_provenance.
- NP698487.RAv2pE1TUrcNn1wdQRvYyEvL0XjGpZyuFv3U9WHpIK8_Y130_assertion wasDerivedFrom befree-20150227 NP698487.RAv2pE1TUrcNn1wdQRvYyEvL0XjGpZyuFv3U9WHpIK8_Y130_provenance.
- NP698487.RAv2pE1TUrcNn1wdQRvYyEvL0XjGpZyuFv3U9WHpIK8_Y130_assertion SIO_000772 25411502 NP698487.RAv2pE1TUrcNn1wdQRvYyEvL0XjGpZyuFv3U9WHpIK8_Y130_provenance.
- NP698487.RAv2pE1TUrcNn1wdQRvYyEvL0XjGpZyuFv3U9WHpIK8_Y130_assertion evidence source_evidence_literature NP698487.RAv2pE1TUrcNn1wdQRvYyEvL0XjGpZyuFv3U9WHpIK8_Y130_provenance.
- NP698487.RAv2pE1TUrcNn1wdQRvYyEvL0XjGpZyuFv3U9WHpIK8_Y130_assertion description "[All participants were genotyped for two putatively functional tandem repeat polymorphisms of the dopamine transporter gene (DAT1; SLC6A3), which are argued to influence the level of available synaptic dopamine and confer risk to disorders of inattention.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698487.RAv2pE1TUrcNn1wdQRvYyEvL0XjGpZyuFv3U9WHpIK8_Y130_provenance.