Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP847966.RAU2ipk0pyB_eIxmZIX4wZ8B6sWWDEihMOCw3FHktMS9A130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP847966.RAU2ipk0pyB_eIxmZIX4wZ8B6sWWDEihMOCw3FHktMS9A130_assertion type Assertion NP847966.RAU2ipk0pyB_eIxmZIX4wZ8B6sWWDEihMOCw3FHktMS9A130_head.
- NP847966.RAU2ipk0pyB_eIxmZIX4wZ8B6sWWDEihMOCw3FHktMS9A130_assertion description "[Walker-Warburg Syndrome (WWS) and muscle-eye-brain disease (MEB) are caused by mutations in two genes involved in O-mannosylation, POMT1 and POMGnT1, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP847966.RAU2ipk0pyB_eIxmZIX4wZ8B6sWWDEihMOCw3FHktMS9A130_provenance.
- NP847966.RAU2ipk0pyB_eIxmZIX4wZ8B6sWWDEihMOCw3FHktMS9A130_assertion evidence source_evidence_literature NP847966.RAU2ipk0pyB_eIxmZIX4wZ8B6sWWDEihMOCw3FHktMS9A130_provenance.
- NP847966.RAU2ipk0pyB_eIxmZIX4wZ8B6sWWDEihMOCw3FHktMS9A130_assertion SIO_000772 12925572 NP847966.RAU2ipk0pyB_eIxmZIX4wZ8B6sWWDEihMOCw3FHktMS9A130_provenance.
- NP847966.RAU2ipk0pyB_eIxmZIX4wZ8B6sWWDEihMOCw3FHktMS9A130_assertion wasDerivedFrom befree-20150227 NP847966.RAU2ipk0pyB_eIxmZIX4wZ8B6sWWDEihMOCw3FHktMS9A130_provenance.
- NP847966.RAU2ipk0pyB_eIxmZIX4wZ8B6sWWDEihMOCw3FHktMS9A130_assertion wasGeneratedBy ECO_0000203 NP847966.RAU2ipk0pyB_eIxmZIX4wZ8B6sWWDEihMOCw3FHktMS9A130_provenance.