Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP811445.RAazIwEkOCMCF_qlQxeypvgXVM5CsfCaXnQ-vW14YeBVc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP811445.RAazIwEkOCMCF_qlQxeypvgXVM5CsfCaXnQ-vW14YeBVc130_assertion type Assertion NP811445.RAazIwEkOCMCF_qlQxeypvgXVM5CsfCaXnQ-vW14YeBVc130_head.
- NP811445.RAazIwEkOCMCF_qlQxeypvgXVM5CsfCaXnQ-vW14YeBVc130_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." NP811445.RAazIwEkOCMCF_qlQxeypvgXVM5CsfCaXnQ-vW14YeBVc130_provenance.
- NP811445.RAazIwEkOCMCF_qlQxeypvgXVM5CsfCaXnQ-vW14YeBVc130_assertion evidence source_evidence_literature NP811445.RAazIwEkOCMCF_qlQxeypvgXVM5CsfCaXnQ-vW14YeBVc130_provenance.
- NP811445.RAazIwEkOCMCF_qlQxeypvgXVM5CsfCaXnQ-vW14YeBVc130_assertion SIO_000772 23065719 NP811445.RAazIwEkOCMCF_qlQxeypvgXVM5CsfCaXnQ-vW14YeBVc130_provenance.
- NP811445.RAazIwEkOCMCF_qlQxeypvgXVM5CsfCaXnQ-vW14YeBVc130_assertion wasDerivedFrom befree-20150227 NP811445.RAazIwEkOCMCF_qlQxeypvgXVM5CsfCaXnQ-vW14YeBVc130_provenance.
- NP811445.RAazIwEkOCMCF_qlQxeypvgXVM5CsfCaXnQ-vW14YeBVc130_assertion wasGeneratedBy ECO_0000203 NP811445.RAazIwEkOCMCF_qlQxeypvgXVM5CsfCaXnQ-vW14YeBVc130_provenance.