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- NP465203.RA03rU2OWYTMEq20tTqv4lk79pe25y8yThun73HxlYDUE130_assertion type Assertion NP465203.RA03rU2OWYTMEq20tTqv4lk79pe25y8yThun73HxlYDUE130_head.
- NP465203.RA03rU2OWYTMEq20tTqv4lk79pe25y8yThun73HxlYDUE130_assertion wasGeneratedBy ECO_0000203 NP465203.RA03rU2OWYTMEq20tTqv4lk79pe25y8yThun73HxlYDUE130_provenance.
- NP465203.RA03rU2OWYTMEq20tTqv4lk79pe25y8yThun73HxlYDUE130_assertion wasDerivedFrom befree-20140225 NP465203.RA03rU2OWYTMEq20tTqv4lk79pe25y8yThun73HxlYDUE130_provenance.
- NP465203.RA03rU2OWYTMEq20tTqv4lk79pe25y8yThun73HxlYDUE130_assertion SIO_000772 14551354 NP465203.RA03rU2OWYTMEq20tTqv4lk79pe25y8yThun73HxlYDUE130_provenance.
- NP465203.RA03rU2OWYTMEq20tTqv4lk79pe25y8yThun73HxlYDUE130_assertion evidence source_evidence_literature NP465203.RA03rU2OWYTMEq20tTqv4lk79pe25y8yThun73HxlYDUE130_provenance.
- NP465203.RA03rU2OWYTMEq20tTqv4lk79pe25y8yThun73HxlYDUE130_assertion description "[In a Turkish family, we identified a novel point mutation in the XDH gene responsible for classical type I xanthinuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465203.RA03rU2OWYTMEq20tTqv4lk79pe25y8yThun73HxlYDUE130_provenance.