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- NP651841.RAQRVNU4YyqgkqtBubnoofUKhHdTbLeLuR-tfhjJk61uY130_assertion type Assertion NP651841.RAQRVNU4YyqgkqtBubnoofUKhHdTbLeLuR-tfhjJk61uY130_head.
- NP651841.RAQRVNU4YyqgkqtBubnoofUKhHdTbLeLuR-tfhjJk61uY130_assertion description "[Crouzon Syndrome is an autosomal dominant syndromic craniosynostosis characterized by premature closure of cranial sutures, exophthalmos, and midface hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651841.RAQRVNU4YyqgkqtBubnoofUKhHdTbLeLuR-tfhjJk61uY130_provenance.
- NP651841.RAQRVNU4YyqgkqtBubnoofUKhHdTbLeLuR-tfhjJk61uY130_assertion evidence source_evidence_literature NP651841.RAQRVNU4YyqgkqtBubnoofUKhHdTbLeLuR-tfhjJk61uY130_provenance.
- NP651841.RAQRVNU4YyqgkqtBubnoofUKhHdTbLeLuR-tfhjJk61uY130_assertion SIO_000772 15916101 NP651841.RAQRVNU4YyqgkqtBubnoofUKhHdTbLeLuR-tfhjJk61uY130_provenance.
- NP651841.RAQRVNU4YyqgkqtBubnoofUKhHdTbLeLuR-tfhjJk61uY130_assertion wasDerivedFrom befree-20140225 NP651841.RAQRVNU4YyqgkqtBubnoofUKhHdTbLeLuR-tfhjJk61uY130_provenance.
- NP651841.RAQRVNU4YyqgkqtBubnoofUKhHdTbLeLuR-tfhjJk61uY130_assertion wasGeneratedBy ECO_0000203 NP651841.RAQRVNU4YyqgkqtBubnoofUKhHdTbLeLuR-tfhjJk61uY130_provenance.