Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_assertion> ?p ?o ?g. }
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- NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_assertion type Assertion NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_head.
- NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_assertion description "[Although our data provide no overall support for association of CDH2 rare variants in these disorders considered as single entities, the clinical features and severity of probands carrying the uncommon non-synonymous variants suggest that CDH2, along with other cadherin and cell adhesion genes, is an interesting gene to pursue as a plausible contributor to OCD, TD and related disorders with repetitive behaviors, including autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_provenance.
- NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_assertion evidence source_evidence_literature NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_provenance.
- NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_assertion SIO_000772 23321619 NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_provenance.
- NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_assertion wasDerivedFrom befree-20140225 NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_provenance.
- NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_assertion wasGeneratedBy ECO_0000203 NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_provenance.