Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP581725.RAz4zGbNSS56tNec04dZnWQcK48ByytJLRgPMuyW-Smuo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP581725.RAz4zGbNSS56tNec04dZnWQcK48ByytJLRgPMuyW-Smuo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP581725.RAz4zGbNSS56tNec04dZnWQcK48ByytJLRgPMuyW-Smuo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP581725.RAz4zGbNSS56tNec04dZnWQcK48ByytJLRgPMuyW-Smuo130_provenance.
- NP581725.RAz4zGbNSS56tNec04dZnWQcK48ByytJLRgPMuyW-Smuo130_assertion description "[Higher burdens of rare, potentially deleterious variants were identified in autism cases for three pathway genes previously implicated in syndromic autism spectrum disorder, TSC1, TSC2, and SHANK3, suggesting that genetic variation in these genes also contributes to risk for non-syndromic autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581725.RAz4zGbNSS56tNec04dZnWQcK48ByytJLRgPMuyW-Smuo130_provenance.
- NP581725.RAz4zGbNSS56tNec04dZnWQcK48ByytJLRgPMuyW-Smuo130_assertion evidence source_evidence_literature NP581725.RAz4zGbNSS56tNec04dZnWQcK48ByytJLRgPMuyW-Smuo130_provenance.
- NP581725.RAz4zGbNSS56tNec04dZnWQcK48ByytJLRgPMuyW-Smuo130_assertion SIO_000772 22558107 NP581725.RAz4zGbNSS56tNec04dZnWQcK48ByytJLRgPMuyW-Smuo130_provenance.
- NP581725.RAz4zGbNSS56tNec04dZnWQcK48ByytJLRgPMuyW-Smuo130_assertion wasDerivedFrom befree-20140225 NP581725.RAz4zGbNSS56tNec04dZnWQcK48ByytJLRgPMuyW-Smuo130_provenance.
- NP581725.RAz4zGbNSS56tNec04dZnWQcK48ByytJLRgPMuyW-Smuo130_assertion wasGeneratedBy ECO_0000203 NP581725.RAz4zGbNSS56tNec04dZnWQcK48ByytJLRgPMuyW-Smuo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP581725.RAz4zGbNSS56tNec04dZnWQcK48ByytJLRgPMuyW-Smuo130_provenance.