Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_provenance.
- NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_assertion wasGeneratedBy ECO_0000203 NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_provenance.
- NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_assertion wasDerivedFrom befree-20150227 NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_provenance.
- NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_assertion SIO_000772 23350639 NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_provenance.
- NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_assertion evidence source_evidence_literature NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_provenance.
- NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_assertion description "[Co-occurrence of a de novo SHANK2 mutation and a CHRNA7 duplication in two reported patients with ASD and ID as well as in the patient with t(11;17;19), severe ID and behavior problems suggests convergence of these genes on a common synaptic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_provenance.