Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1044172.RAFwhHVvELfutL5YJivsshvxlTHBZ_iwiNvrcA0wzjufY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1044172.RAFwhHVvELfutL5YJivsshvxlTHBZ_iwiNvrcA0wzjufY130_assertion type Assertion NP1044172.RAFwhHVvELfutL5YJivsshvxlTHBZ_iwiNvrcA0wzjufY130_head.
- NP1044172.RAFwhHVvELfutL5YJivsshvxlTHBZ_iwiNvrcA0wzjufY130_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." NP1044172.RAFwhHVvELfutL5YJivsshvxlTHBZ_iwiNvrcA0wzjufY130_provenance.
- NP1044172.RAFwhHVvELfutL5YJivsshvxlTHBZ_iwiNvrcA0wzjufY130_assertion evidence source_evidence_literature NP1044172.RAFwhHVvELfutL5YJivsshvxlTHBZ_iwiNvrcA0wzjufY130_provenance.
- NP1044172.RAFwhHVvELfutL5YJivsshvxlTHBZ_iwiNvrcA0wzjufY130_assertion SIO_000772 23321619 NP1044172.RAFwhHVvELfutL5YJivsshvxlTHBZ_iwiNvrcA0wzjufY130_provenance.
- NP1044172.RAFwhHVvELfutL5YJivsshvxlTHBZ_iwiNvrcA0wzjufY130_assertion wasDerivedFrom befree-2016 NP1044172.RAFwhHVvELfutL5YJivsshvxlTHBZ_iwiNvrcA0wzjufY130_provenance.
- NP1044172.RAFwhHVvELfutL5YJivsshvxlTHBZ_iwiNvrcA0wzjufY130_assertion wasGeneratedBy ECO_0000203 NP1044172.RAFwhHVvELfutL5YJivsshvxlTHBZ_iwiNvrcA0wzjufY130_provenance.