Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP811436.RAOfFSPXzpKe64jvTjxqGQdhG1zxfWTGb5yfArDH9I8pg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP811436.RAOfFSPXzpKe64jvTjxqGQdhG1zxfWTGb5yfArDH9I8pg130_assertion type Assertion NP811436.RAOfFSPXzpKe64jvTjxqGQdhG1zxfWTGb5yfArDH9I8pg130_head.
- NP811436.RAOfFSPXzpKe64jvTjxqGQdhG1zxfWTGb5yfArDH9I8pg130_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." NP811436.RAOfFSPXzpKe64jvTjxqGQdhG1zxfWTGb5yfArDH9I8pg130_provenance.
- NP811436.RAOfFSPXzpKe64jvTjxqGQdhG1zxfWTGb5yfArDH9I8pg130_assertion evidence source_evidence_literature NP811436.RAOfFSPXzpKe64jvTjxqGQdhG1zxfWTGb5yfArDH9I8pg130_provenance.
- NP811436.RAOfFSPXzpKe64jvTjxqGQdhG1zxfWTGb5yfArDH9I8pg130_assertion SIO_000772 23065719 NP811436.RAOfFSPXzpKe64jvTjxqGQdhG1zxfWTGb5yfArDH9I8pg130_provenance.
- NP811436.RAOfFSPXzpKe64jvTjxqGQdhG1zxfWTGb5yfArDH9I8pg130_assertion wasDerivedFrom befree-20150227 NP811436.RAOfFSPXzpKe64jvTjxqGQdhG1zxfWTGb5yfArDH9I8pg130_provenance.
- NP811436.RAOfFSPXzpKe64jvTjxqGQdhG1zxfWTGb5yfArDH9I8pg130_assertion wasGeneratedBy ECO_0000203 NP811436.RAOfFSPXzpKe64jvTjxqGQdhG1zxfWTGb5yfArDH9I8pg130_provenance.