Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1139726.RAZzYuiIGI4VPHJqQyYX71gEUZu5xRyB4dTlOo_ZnscQ0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1139726.RAZzYuiIGI4VPHJqQyYX71gEUZu5xRyB4dTlOo_ZnscQ0130_assertion type Assertion NP1139726.RAZzYuiIGI4VPHJqQyYX71gEUZu5xRyB4dTlOo_ZnscQ0130_head.
- NP1139726.RAZzYuiIGI4VPHJqQyYX71gEUZu5xRyB4dTlOo_ZnscQ0130_assertion description "[The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1139726.RAZzYuiIGI4VPHJqQyYX71gEUZu5xRyB4dTlOo_ZnscQ0130_provenance.
- NP1139726.RAZzYuiIGI4VPHJqQyYX71gEUZu5xRyB4dTlOo_ZnscQ0130_assertion evidence source_evidence_literature NP1139726.RAZzYuiIGI4VPHJqQyYX71gEUZu5xRyB4dTlOo_ZnscQ0130_provenance.
- NP1139726.RAZzYuiIGI4VPHJqQyYX71gEUZu5xRyB4dTlOo_ZnscQ0130_assertion SIO_000772 24369382 NP1139726.RAZzYuiIGI4VPHJqQyYX71gEUZu5xRyB4dTlOo_ZnscQ0130_provenance.
- NP1139726.RAZzYuiIGI4VPHJqQyYX71gEUZu5xRyB4dTlOo_ZnscQ0130_assertion wasDerivedFrom befree-2016 NP1139726.RAZzYuiIGI4VPHJqQyYX71gEUZu5xRyB4dTlOo_ZnscQ0130_provenance.
- NP1139726.RAZzYuiIGI4VPHJqQyYX71gEUZu5xRyB4dTlOo_ZnscQ0130_assertion wasGeneratedBy ECO_0000203 NP1139726.RAZzYuiIGI4VPHJqQyYX71gEUZu5xRyB4dTlOo_ZnscQ0130_provenance.