Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP431720.RA3I8fFAzw4-12UOGM2Z9JeqgzaMPKCmFx50IYVhoBdpU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP431720.RA3I8fFAzw4-12UOGM2Z9JeqgzaMPKCmFx50IYVhoBdpU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP431720.RA3I8fFAzw4-12UOGM2Z9JeqgzaMPKCmFx50IYVhoBdpU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP431720.RA3I8fFAzw4-12UOGM2Z9JeqgzaMPKCmFx50IYVhoBdpU130_provenance.
- NP431720.RA3I8fFAzw4-12UOGM2Z9JeqgzaMPKCmFx50IYVhoBdpU130_assertion description "[When haplotype TDT analysis of HTR4 was performed, we further found that the C/G haplotype of the 83097 C>T and 83198 A>G polymorphisms (chi(2)=8.783, P=0.003) and the C/G/C haplotype of these and the -36 C>T polymorphism (chi(2)=5.762, P=0.016) were under-transmitted to probands with ADHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431720.RA3I8fFAzw4-12UOGM2Z9JeqgzaMPKCmFx50IYVhoBdpU130_provenance.
- NP431720.RA3I8fFAzw4-12UOGM2Z9JeqgzaMPKCmFx50IYVhoBdpU130_assertion evidence source_evidence_literature NP431720.RA3I8fFAzw4-12UOGM2Z9JeqgzaMPKCmFx50IYVhoBdpU130_provenance.
- NP431720.RA3I8fFAzw4-12UOGM2Z9JeqgzaMPKCmFx50IYVhoBdpU130_assertion SIO_000772 16563621 NP431720.RA3I8fFAzw4-12UOGM2Z9JeqgzaMPKCmFx50IYVhoBdpU130_provenance.
- NP431720.RA3I8fFAzw4-12UOGM2Z9JeqgzaMPKCmFx50IYVhoBdpU130_assertion wasDerivedFrom befree-20140225 NP431720.RA3I8fFAzw4-12UOGM2Z9JeqgzaMPKCmFx50IYVhoBdpU130_provenance.
- NP431720.RA3I8fFAzw4-12UOGM2Z9JeqgzaMPKCmFx50IYVhoBdpU130_assertion wasGeneratedBy ECO_0000203 NP431720.RA3I8fFAzw4-12UOGM2Z9JeqgzaMPKCmFx50IYVhoBdpU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP431720.RA3I8fFAzw4-12UOGM2Z9JeqgzaMPKCmFx50IYVhoBdpU130_provenance.