Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP718109.RA1WEXY_vphZ3L1Sp7kg1BtZ37FotLz8qko_fYbaGdb4k130_assertion> ?p ?o ?g. }
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- NP718109.RA1WEXY_vphZ3L1Sp7kg1BtZ37FotLz8qko_fYbaGdb4k130_assertion type Assertion NP718109.RA1WEXY_vphZ3L1Sp7kg1BtZ37FotLz8qko_fYbaGdb4k130_head.
- NP718109.RA1WEXY_vphZ3L1Sp7kg1BtZ37FotLz8qko_fYbaGdb4k130_assertion description "[To date POMT2 mutations have been identified in CMD cases with a wide range of clinical severities from Walker-Warburg syndrome to limb girdle muscular dystrophy without structural brain or ocular involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718109.RA1WEXY_vphZ3L1Sp7kg1BtZ37FotLz8qko_fYbaGdb4k130_provenance.
- NP718109.RA1WEXY_vphZ3L1Sp7kg1BtZ37FotLz8qko_fYbaGdb4k130_assertion evidence source_evidence_literature NP718109.RA1WEXY_vphZ3L1Sp7kg1BtZ37FotLz8qko_fYbaGdb4k130_provenance.
- NP718109.RA1WEXY_vphZ3L1Sp7kg1BtZ37FotLz8qko_fYbaGdb4k130_assertion SIO_000772 19138766 NP718109.RA1WEXY_vphZ3L1Sp7kg1BtZ37FotLz8qko_fYbaGdb4k130_provenance.
- NP718109.RA1WEXY_vphZ3L1Sp7kg1BtZ37FotLz8qko_fYbaGdb4k130_assertion wasDerivedFrom befree-20140225 NP718109.RA1WEXY_vphZ3L1Sp7kg1BtZ37FotLz8qko_fYbaGdb4k130_provenance.
- NP718109.RA1WEXY_vphZ3L1Sp7kg1BtZ37FotLz8qko_fYbaGdb4k130_assertion wasGeneratedBy ECO_0000203 NP718109.RA1WEXY_vphZ3L1Sp7kg1BtZ37FotLz8qko_fYbaGdb4k130_provenance.