Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP902631.RALYlXmcx4P_CmpKOUbceq09YTBMU1FRWCqhxDEwHKImY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP902631.RALYlXmcx4P_CmpKOUbceq09YTBMU1FRWCqhxDEwHKImY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP902631.RALYlXmcx4P_CmpKOUbceq09YTBMU1FRWCqhxDEwHKImY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP902631.RALYlXmcx4P_CmpKOUbceq09YTBMU1FRWCqhxDEwHKImY130_provenance.
- NP902631.RALYlXmcx4P_CmpKOUbceq09YTBMU1FRWCqhxDEwHKImY130_assertion description "[To analyze whether genetic variants in the OXTR gene are associated with ASD we performed family-based single-marker and haplotype association analyses with 22 single nucleotide polymorphisms (SNPs) in the OXTR and its 5' region in 100 families with autistic disorders on high-functioning level (Asperger syndrome (AS), high-functioning autism (HFA), and atypical autism (AA)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902631.RALYlXmcx4P_CmpKOUbceq09YTBMU1FRWCqhxDEwHKImY130_provenance.
- NP902631.RALYlXmcx4P_CmpKOUbceq09YTBMU1FRWCqhxDEwHKImY130_assertion evidence source_evidence_literature NP902631.RALYlXmcx4P_CmpKOUbceq09YTBMU1FRWCqhxDEwHKImY130_provenance.
- NP902631.RALYlXmcx4P_CmpKOUbceq09YTBMU1FRWCqhxDEwHKImY130_assertion SIO_000772 19777562 NP902631.RALYlXmcx4P_CmpKOUbceq09YTBMU1FRWCqhxDEwHKImY130_provenance.
- NP902631.RALYlXmcx4P_CmpKOUbceq09YTBMU1FRWCqhxDEwHKImY130_assertion wasDerivedFrom befree-20140225 NP902631.RALYlXmcx4P_CmpKOUbceq09YTBMU1FRWCqhxDEwHKImY130_provenance.
- NP902631.RALYlXmcx4P_CmpKOUbceq09YTBMU1FRWCqhxDEwHKImY130_assertion wasGeneratedBy ECO_0000203 NP902631.RALYlXmcx4P_CmpKOUbceq09YTBMU1FRWCqhxDEwHKImY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP902631.RALYlXmcx4P_CmpKOUbceq09YTBMU1FRWCqhxDEwHKImY130_provenance.