Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP630706.RAWkFHCtrecZQwcjjBHfZJzAtAp5p2CJKD25rUohnqPXs130_assertion> ?p ?o ?g. }
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- NP630706.RAWkFHCtrecZQwcjjBHfZJzAtAp5p2CJKD25rUohnqPXs130_assertion type Assertion NP630706.RAWkFHCtrecZQwcjjBHfZJzAtAp5p2CJKD25rUohnqPXs130_head.
- NP630706.RAWkFHCtrecZQwcjjBHfZJzAtAp5p2CJKD25rUohnqPXs130_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." NP630706.RAWkFHCtrecZQwcjjBHfZJzAtAp5p2CJKD25rUohnqPXs130_provenance.
- NP630706.RAWkFHCtrecZQwcjjBHfZJzAtAp5p2CJKD25rUohnqPXs130_assertion evidence source_evidence_literature NP630706.RAWkFHCtrecZQwcjjBHfZJzAtAp5p2CJKD25rUohnqPXs130_provenance.
- NP630706.RAWkFHCtrecZQwcjjBHfZJzAtAp5p2CJKD25rUohnqPXs130_assertion SIO_000772 17878207 NP630706.RAWkFHCtrecZQwcjjBHfZJzAtAp5p2CJKD25rUohnqPXs130_provenance.
- NP630706.RAWkFHCtrecZQwcjjBHfZJzAtAp5p2CJKD25rUohnqPXs130_assertion wasDerivedFrom befree-2016 NP630706.RAWkFHCtrecZQwcjjBHfZJzAtAp5p2CJKD25rUohnqPXs130_provenance.
- NP630706.RAWkFHCtrecZQwcjjBHfZJzAtAp5p2CJKD25rUohnqPXs130_assertion wasGeneratedBy ECO_0000203 NP630706.RAWkFHCtrecZQwcjjBHfZJzAtAp5p2CJKD25rUohnqPXs130_provenance.