Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP921786.RAfjmHPXAz4oB-j9kEZebbH3XKGm-MPpmSu_krP61llQM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP921786.RAfjmHPXAz4oB-j9kEZebbH3XKGm-MPpmSu_krP61llQM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP921786.RAfjmHPXAz4oB-j9kEZebbH3XKGm-MPpmSu_krP61llQM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP921786.RAfjmHPXAz4oB-j9kEZebbH3XKGm-MPpmSu_krP61llQM130_provenance.
- NP921786.RAfjmHPXAz4oB-j9kEZebbH3XKGm-MPpmSu_krP61llQM130_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." NP921786.RAfjmHPXAz4oB-j9kEZebbH3XKGm-MPpmSu_krP61llQM130_provenance.
- NP921786.RAfjmHPXAz4oB-j9kEZebbH3XKGm-MPpmSu_krP61llQM130_assertion evidence source_evidence_literature NP921786.RAfjmHPXAz4oB-j9kEZebbH3XKGm-MPpmSu_krP61llQM130_provenance.
- NP921786.RAfjmHPXAz4oB-j9kEZebbH3XKGm-MPpmSu_krP61llQM130_assertion SIO_000772 25411502 NP921786.RAfjmHPXAz4oB-j9kEZebbH3XKGm-MPpmSu_krP61llQM130_provenance.
- NP921786.RAfjmHPXAz4oB-j9kEZebbH3XKGm-MPpmSu_krP61llQM130_assertion wasDerivedFrom befree-20150227 NP921786.RAfjmHPXAz4oB-j9kEZebbH3XKGm-MPpmSu_krP61llQM130_provenance.
- NP921786.RAfjmHPXAz4oB-j9kEZebbH3XKGm-MPpmSu_krP61llQM130_assertion wasGeneratedBy ECO_0000203 NP921786.RAfjmHPXAz4oB-j9kEZebbH3XKGm-MPpmSu_krP61llQM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP921786.RAfjmHPXAz4oB-j9kEZebbH3XKGm-MPpmSu_krP61llQM130_provenance.