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- source_evidence_literature type ECO_0000212 NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_provenance.
- NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_assertion wasGeneratedBy ECO_0000203 NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_provenance.
- NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_assertion wasDerivedFrom befree-20150227 NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_provenance.
- NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_assertion SIO_000772 23350639 NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_provenance.
- NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_assertion evidence source_evidence_literature NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_provenance.
- NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_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." NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_provenance.