Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP382211.RAvF5cgObHjOaJyRYWkD4lw-4hmD9ufvmfwsnquTHjoRk130_assertion> ?p ?o ?g. }
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- NP382211.RAvF5cgObHjOaJyRYWkD4lw-4hmD9ufvmfwsnquTHjoRk130_assertion type Assertion NP382211.RAvF5cgObHjOaJyRYWkD4lw-4hmD9ufvmfwsnquTHjoRk130_head.
- NP382211.RAvF5cgObHjOaJyRYWkD4lw-4hmD9ufvmfwsnquTHjoRk130_assertion description "[The most severe phenotypes are Walker-Warburg Syndrome (WWS) and muscle-eye-brain disease (MEB) presenting with lissencephaly type II (LIS II) and in which muscular dystrophy is associated with mental retardation and eye abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382211.RAvF5cgObHjOaJyRYWkD4lw-4hmD9ufvmfwsnquTHjoRk130_provenance.
- NP382211.RAvF5cgObHjOaJyRYWkD4lw-4hmD9ufvmfwsnquTHjoRk130_assertion evidence source_evidence_literature NP382211.RAvF5cgObHjOaJyRYWkD4lw-4hmD9ufvmfwsnquTHjoRk130_provenance.
- NP382211.RAvF5cgObHjOaJyRYWkD4lw-4hmD9ufvmfwsnquTHjoRk130_assertion SIO_000772 21727005 NP382211.RAvF5cgObHjOaJyRYWkD4lw-4hmD9ufvmfwsnquTHjoRk130_provenance.
- NP382211.RAvF5cgObHjOaJyRYWkD4lw-4hmD9ufvmfwsnquTHjoRk130_assertion wasDerivedFrom befree-20140225 NP382211.RAvF5cgObHjOaJyRYWkD4lw-4hmD9ufvmfwsnquTHjoRk130_provenance.
- NP382211.RAvF5cgObHjOaJyRYWkD4lw-4hmD9ufvmfwsnquTHjoRk130_assertion wasGeneratedBy ECO_0000203 NP382211.RAvF5cgObHjOaJyRYWkD4lw-4hmD9ufvmfwsnquTHjoRk130_provenance.