Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP340634.RA8R8qYvt8eloIspJPJPSRfpSAtK28Gc_EhNI1jfodG1c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP340634.RA8R8qYvt8eloIspJPJPSRfpSAtK28Gc_EhNI1jfodG1c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP340634.RA8R8qYvt8eloIspJPJPSRfpSAtK28Gc_EhNI1jfodG1c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP340634.RA8R8qYvt8eloIspJPJPSRfpSAtK28Gc_EhNI1jfodG1c130_provenance.
- NP340634.RA8R8qYvt8eloIspJPJPSRfpSAtK28Gc_EhNI1jfodG1c130_assertion description "[A specific combination of two COMT and SLC6A2 gene haplotypes, containing the low functioning COMT variant was nominally associated with low ADHD scores in all scales.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP340634.RA8R8qYvt8eloIspJPJPSRfpSAtK28Gc_EhNI1jfodG1c130_provenance.
- NP340634.RA8R8qYvt8eloIspJPJPSRfpSAtK28Gc_EhNI1jfodG1c130_assertion evidence source_evidence_literature NP340634.RA8R8qYvt8eloIspJPJPSRfpSAtK28Gc_EhNI1jfodG1c130_provenance.
- NP340634.RA8R8qYvt8eloIspJPJPSRfpSAtK28Gc_EhNI1jfodG1c130_assertion SIO_000772 17994190 NP340634.RA8R8qYvt8eloIspJPJPSRfpSAtK28Gc_EhNI1jfodG1c130_provenance.
- NP340634.RA8R8qYvt8eloIspJPJPSRfpSAtK28Gc_EhNI1jfodG1c130_assertion wasDerivedFrom befree-20140225 NP340634.RA8R8qYvt8eloIspJPJPSRfpSAtK28Gc_EhNI1jfodG1c130_provenance.
- NP340634.RA8R8qYvt8eloIspJPJPSRfpSAtK28Gc_EhNI1jfodG1c130_assertion wasGeneratedBy ECO_0000203 NP340634.RA8R8qYvt8eloIspJPJPSRfpSAtK28Gc_EhNI1jfodG1c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP340634.RA8R8qYvt8eloIspJPJPSRfpSAtK28Gc_EhNI1jfodG1c130_provenance.