Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP930681.RAawE7QX5vqeHfah1ldPHOS2VVclX7gREiQlPmPmIHG3s130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP930681.RAawE7QX5vqeHfah1ldPHOS2VVclX7gREiQlPmPmIHG3s130_assertion type Assertion NP930681.RAawE7QX5vqeHfah1ldPHOS2VVclX7gREiQlPmPmIHG3s130_head.
- NP930681.RAawE7QX5vqeHfah1ldPHOS2VVclX7gREiQlPmPmIHG3s130_assertion description "[Inherited and de novo SHANK2 variants associated with autism spectrum disorder impair neuronal morphogenesis and physiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP930681.RAawE7QX5vqeHfah1ldPHOS2VVclX7gREiQlPmPmIHG3s130_provenance.
- NP930681.RAawE7QX5vqeHfah1ldPHOS2VVclX7gREiQlPmPmIHG3s130_assertion evidence source_evidence_literature NP930681.RAawE7QX5vqeHfah1ldPHOS2VVclX7gREiQlPmPmIHG3s130_provenance.
- NP930681.RAawE7QX5vqeHfah1ldPHOS2VVclX7gREiQlPmPmIHG3s130_assertion SIO_000772 21994763 NP930681.RAawE7QX5vqeHfah1ldPHOS2VVclX7gREiQlPmPmIHG3s130_provenance.
- NP930681.RAawE7QX5vqeHfah1ldPHOS2VVclX7gREiQlPmPmIHG3s130_assertion wasDerivedFrom befree-2016 NP930681.RAawE7QX5vqeHfah1ldPHOS2VVclX7gREiQlPmPmIHG3s130_provenance.
- NP930681.RAawE7QX5vqeHfah1ldPHOS2VVclX7gREiQlPmPmIHG3s130_assertion wasGeneratedBy ECO_0000203 NP930681.RAawE7QX5vqeHfah1ldPHOS2VVclX7gREiQlPmPmIHG3s130_provenance.