Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP881366.RAGjLKfzvwlOzKid_xZLgQpspNY0xxvTdABOseZ_med0E130_assertion> ?p ?o ?g. }
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- NP881366.RAGjLKfzvwlOzKid_xZLgQpspNY0xxvTdABOseZ_med0E130_assertion type Assertion NP881366.RAGjLKfzvwlOzKid_xZLgQpspNY0xxvTdABOseZ_med0E130_head.
- NP881366.RAGjLKfzvwlOzKid_xZLgQpspNY0xxvTdABOseZ_med0E130_assertion description "[Given the overlap of this autism/mental retardation (MR) phenotype and the MR-associated disorders in our patients, together with the fact that mapping of the additional autosomal breakpoints involved did not disclose obvious candidate disease genes, we ascertain with this study that AUTS2 mutations are clearly linked to autosomal dominant mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881366.RAGjLKfzvwlOzKid_xZLgQpspNY0xxvTdABOseZ_med0E130_provenance.
- NP881366.RAGjLKfzvwlOzKid_xZLgQpspNY0xxvTdABOseZ_med0E130_assertion evidence source_evidence_literature NP881366.RAGjLKfzvwlOzKid_xZLgQpspNY0xxvTdABOseZ_med0E130_provenance.
- NP881366.RAGjLKfzvwlOzKid_xZLgQpspNY0xxvTdABOseZ_med0E130_assertion SIO_000772 17211639 NP881366.RAGjLKfzvwlOzKid_xZLgQpspNY0xxvTdABOseZ_med0E130_provenance.
- NP881366.RAGjLKfzvwlOzKid_xZLgQpspNY0xxvTdABOseZ_med0E130_assertion wasDerivedFrom befree-20150227 NP881366.RAGjLKfzvwlOzKid_xZLgQpspNY0xxvTdABOseZ_med0E130_provenance.
- NP881366.RAGjLKfzvwlOzKid_xZLgQpspNY0xxvTdABOseZ_med0E130_assertion wasGeneratedBy ECO_0000203 NP881366.RAGjLKfzvwlOzKid_xZLgQpspNY0xxvTdABOseZ_med0E130_provenance.