Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_assertion type Assertion NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_head.
- NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_assertion description "[All patients with POMT1 and POMT2 mutations had evidence of either structural or functional central nervous system involvement including four patients with mental retardation and a LGMD phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_provenance.
- NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_assertion evidence source_evidence_literature NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_provenance.
- NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_assertion SIO_000772 17878207 NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_provenance.
- NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_assertion wasDerivedFrom befree-20150227 NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_provenance.
- NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_assertion wasGeneratedBy ECO_0000203 NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_provenance.