Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP742654.RArM4hTzDNmUHy12qq5xL1WySQnJYUomHYBPEBn9jSrg8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP742654.RArM4hTzDNmUHy12qq5xL1WySQnJYUomHYBPEBn9jSrg8130_assertion type Assertion NP742654.RArM4hTzDNmUHy12qq5xL1WySQnJYUomHYBPEBn9jSrg8130_head.
- NP742654.RArM4hTzDNmUHy12qq5xL1WySQnJYUomHYBPEBn9jSrg8130_assertion description "[The phenotypic correlation with the mouse Herc1 and Herc2 mutants as well as the phenotypic overlap with Angelman syndrome provide further evidence that pathogenic changes in HERC2 are associated with nonsyndromic intellectual disability, autism, and gait disturbance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP742654.RArM4hTzDNmUHy12qq5xL1WySQnJYUomHYBPEBn9jSrg8130_provenance.
- NP742654.RArM4hTzDNmUHy12qq5xL1WySQnJYUomHYBPEBn9jSrg8130_assertion evidence source_evidence_literature NP742654.RArM4hTzDNmUHy12qq5xL1WySQnJYUomHYBPEBn9jSrg8130_provenance.
- NP742654.RArM4hTzDNmUHy12qq5xL1WySQnJYUomHYBPEBn9jSrg8130_assertion SIO_000772 23065719 NP742654.RArM4hTzDNmUHy12qq5xL1WySQnJYUomHYBPEBn9jSrg8130_provenance.
- NP742654.RArM4hTzDNmUHy12qq5xL1WySQnJYUomHYBPEBn9jSrg8130_assertion wasDerivedFrom befree-20140225 NP742654.RArM4hTzDNmUHy12qq5xL1WySQnJYUomHYBPEBn9jSrg8130_provenance.
- NP742654.RArM4hTzDNmUHy12qq5xL1WySQnJYUomHYBPEBn9jSrg8130_assertion wasGeneratedBy ECO_0000203 NP742654.RArM4hTzDNmUHy12qq5xL1WySQnJYUomHYBPEBn9jSrg8130_provenance.