Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1021082.RAxv2HEJ_tPMKhhmA8BF_vl58vz1YtTiV4t4AAomm4Yj4130_assertion> ?p ?o ?g. }
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- NP1021082.RAxv2HEJ_tPMKhhmA8BF_vl58vz1YtTiV4t4AAomm4Yj4130_assertion type Assertion NP1021082.RAxv2HEJ_tPMKhhmA8BF_vl58vz1YtTiV4t4AAomm4Yj4130_head.
- NP1021082.RAxv2HEJ_tPMKhhmA8BF_vl58vz1YtTiV4t4AAomm4Yj4130_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." NP1021082.RAxv2HEJ_tPMKhhmA8BF_vl58vz1YtTiV4t4AAomm4Yj4130_provenance.
- NP1021082.RAxv2HEJ_tPMKhhmA8BF_vl58vz1YtTiV4t4AAomm4Yj4130_assertion evidence source_evidence_literature NP1021082.RAxv2HEJ_tPMKhhmA8BF_vl58vz1YtTiV4t4AAomm4Yj4130_provenance.
- NP1021082.RAxv2HEJ_tPMKhhmA8BF_vl58vz1YtTiV4t4AAomm4Yj4130_assertion SIO_000772 23065719 NP1021082.RAxv2HEJ_tPMKhhmA8BF_vl58vz1YtTiV4t4AAomm4Yj4130_provenance.
- NP1021082.RAxv2HEJ_tPMKhhmA8BF_vl58vz1YtTiV4t4AAomm4Yj4130_assertion wasDerivedFrom befree-2016 NP1021082.RAxv2HEJ_tPMKhhmA8BF_vl58vz1YtTiV4t4AAomm4Yj4130_provenance.
- NP1021082.RAxv2HEJ_tPMKhhmA8BF_vl58vz1YtTiV4t4AAomm4Yj4130_assertion wasGeneratedBy ECO_0000203 NP1021082.RAxv2HEJ_tPMKhhmA8BF_vl58vz1YtTiV4t4AAomm4Yj4130_provenance.