Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP765645.RADAenF6FUat1qMEDsXvt33V8B8GvT3ixgGFlZpFEciX8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP765645.RADAenF6FUat1qMEDsXvt33V8B8GvT3ixgGFlZpFEciX8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP765645.RADAenF6FUat1qMEDsXvt33V8B8GvT3ixgGFlZpFEciX8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP765645.RADAenF6FUat1qMEDsXvt33V8B8GvT3ixgGFlZpFEciX8130_provenance.
- NP765645.RADAenF6FUat1qMEDsXvt33V8B8GvT3ixgGFlZpFEciX8130_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." NP765645.RADAenF6FUat1qMEDsXvt33V8B8GvT3ixgGFlZpFEciX8130_provenance.
- NP765645.RADAenF6FUat1qMEDsXvt33V8B8GvT3ixgGFlZpFEciX8130_assertion evidence source_evidence_literature NP765645.RADAenF6FUat1qMEDsXvt33V8B8GvT3ixgGFlZpFEciX8130_provenance.
- NP765645.RADAenF6FUat1qMEDsXvt33V8B8GvT3ixgGFlZpFEciX8130_assertion SIO_000772 22558107 NP765645.RADAenF6FUat1qMEDsXvt33V8B8GvT3ixgGFlZpFEciX8130_provenance.
- NP765645.RADAenF6FUat1qMEDsXvt33V8B8GvT3ixgGFlZpFEciX8130_assertion wasDerivedFrom befree-20140225 NP765645.RADAenF6FUat1qMEDsXvt33V8B8GvT3ixgGFlZpFEciX8130_provenance.
- NP765645.RADAenF6FUat1qMEDsXvt33V8B8GvT3ixgGFlZpFEciX8130_assertion wasGeneratedBy ECO_0000203 NP765645.RADAenF6FUat1qMEDsXvt33V8B8GvT3ixgGFlZpFEciX8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP765645.RADAenF6FUat1qMEDsXvt33V8B8GvT3ixgGFlZpFEciX8130_provenance.