Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP604653.RAGB2HRGw2rdIqGzhEv2eb4zT-XmeMiD8qIjcnmpAzA5U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP604653.RAGB2HRGw2rdIqGzhEv2eb4zT-XmeMiD8qIjcnmpAzA5U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP604653.RAGB2HRGw2rdIqGzhEv2eb4zT-XmeMiD8qIjcnmpAzA5U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP604653.RAGB2HRGw2rdIqGzhEv2eb4zT-XmeMiD8qIjcnmpAzA5U130_provenance.
- NP604653.RAGB2HRGw2rdIqGzhEv2eb4zT-XmeMiD8qIjcnmpAzA5U130_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." NP604653.RAGB2HRGw2rdIqGzhEv2eb4zT-XmeMiD8qIjcnmpAzA5U130_provenance.
- NP604653.RAGB2HRGw2rdIqGzhEv2eb4zT-XmeMiD8qIjcnmpAzA5U130_assertion evidence source_evidence_literature NP604653.RAGB2HRGw2rdIqGzhEv2eb4zT-XmeMiD8qIjcnmpAzA5U130_provenance.
- NP604653.RAGB2HRGw2rdIqGzhEv2eb4zT-XmeMiD8qIjcnmpAzA5U130_assertion SIO_000772 19777562 NP604653.RAGB2HRGw2rdIqGzhEv2eb4zT-XmeMiD8qIjcnmpAzA5U130_provenance.
- NP604653.RAGB2HRGw2rdIqGzhEv2eb4zT-XmeMiD8qIjcnmpAzA5U130_assertion wasDerivedFrom befree-20150227 NP604653.RAGB2HRGw2rdIqGzhEv2eb4zT-XmeMiD8qIjcnmpAzA5U130_provenance.
- NP604653.RAGB2HRGw2rdIqGzhEv2eb4zT-XmeMiD8qIjcnmpAzA5U130_assertion wasGeneratedBy ECO_0000203 NP604653.RAGB2HRGw2rdIqGzhEv2eb4zT-XmeMiD8qIjcnmpAzA5U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP604653.RAGB2HRGw2rdIqGzhEv2eb4zT-XmeMiD8qIjcnmpAzA5U130_provenance.