Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP895095.RAGZZPbnjqgY47fPxCuvGsbq0nUjU5IwmhPcugFgPqSYo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP895095.RAGZZPbnjqgY47fPxCuvGsbq0nUjU5IwmhPcugFgPqSYo130_assertion type Assertion NP895095.RAGZZPbnjqgY47fPxCuvGsbq0nUjU5IwmhPcugFgPqSYo130_head.
- NP895095.RAGZZPbnjqgY47fPxCuvGsbq0nUjU5IwmhPcugFgPqSYo130_assertion description "[Within this group mutations in the protein O-mannosyltransferase genes (POMT1 and POMT2) are known to cause a spectrum of CMD disorders including the Walker-Warburg Syndrome with severe brain and ocular malformations, and the limb girdle muscular dystrophy with and without mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895095.RAGZZPbnjqgY47fPxCuvGsbq0nUjU5IwmhPcugFgPqSYo130_provenance.
- NP895095.RAGZZPbnjqgY47fPxCuvGsbq0nUjU5IwmhPcugFgPqSYo130_assertion evidence source_evidence_literature NP895095.RAGZZPbnjqgY47fPxCuvGsbq0nUjU5IwmhPcugFgPqSYo130_provenance.
- NP895095.RAGZZPbnjqgY47fPxCuvGsbq0nUjU5IwmhPcugFgPqSYo130_assertion SIO_000772 24556424 NP895095.RAGZZPbnjqgY47fPxCuvGsbq0nUjU5IwmhPcugFgPqSYo130_provenance.
- NP895095.RAGZZPbnjqgY47fPxCuvGsbq0nUjU5IwmhPcugFgPqSYo130_assertion wasDerivedFrom befree-20150227 NP895095.RAGZZPbnjqgY47fPxCuvGsbq0nUjU5IwmhPcugFgPqSYo130_provenance.
- NP895095.RAGZZPbnjqgY47fPxCuvGsbq0nUjU5IwmhPcugFgPqSYo130_assertion wasGeneratedBy ECO_0000203 NP895095.RAGZZPbnjqgY47fPxCuvGsbq0nUjU5IwmhPcugFgPqSYo130_provenance.