Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP541965.RAlCWJci269ulzk_xJKQCagDnKUbwAa4To7rOfNchZNEg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP541965.RAlCWJci269ulzk_xJKQCagDnKUbwAa4To7rOfNchZNEg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541965.RAlCWJci269ulzk_xJKQCagDnKUbwAa4To7rOfNchZNEg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541965.RAlCWJci269ulzk_xJKQCagDnKUbwAa4To7rOfNchZNEg130_provenance.
- NP541965.RAlCWJci269ulzk_xJKQCagDnKUbwAa4To7rOfNchZNEg130_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." NP541965.RAlCWJci269ulzk_xJKQCagDnKUbwAa4To7rOfNchZNEg130_provenance.
- NP541965.RAlCWJci269ulzk_xJKQCagDnKUbwAa4To7rOfNchZNEg130_assertion evidence source_evidence_literature NP541965.RAlCWJci269ulzk_xJKQCagDnKUbwAa4To7rOfNchZNEg130_provenance.
- NP541965.RAlCWJci269ulzk_xJKQCagDnKUbwAa4To7rOfNchZNEg130_assertion SIO_000772 16563621 NP541965.RAlCWJci269ulzk_xJKQCagDnKUbwAa4To7rOfNchZNEg130_provenance.
- NP541965.RAlCWJci269ulzk_xJKQCagDnKUbwAa4To7rOfNchZNEg130_assertion wasDerivedFrom befree-2016 NP541965.RAlCWJci269ulzk_xJKQCagDnKUbwAa4To7rOfNchZNEg130_provenance.
- NP541965.RAlCWJci269ulzk_xJKQCagDnKUbwAa4To7rOfNchZNEg130_assertion wasGeneratedBy ECO_0000203 NP541965.RAlCWJci269ulzk_xJKQCagDnKUbwAa4To7rOfNchZNEg130_provenance.
- befree-2016 importedOn "2016-02-19" NP541965.RAlCWJci269ulzk_xJKQCagDnKUbwAa4To7rOfNchZNEg130_provenance.