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- NP502625.RAp3rPopBruIBrpwr-VnEU1knGul2snWxhi9qVaoo0pBQ130_assertion type Assertion NP502625.RAp3rPopBruIBrpwr-VnEU1knGul2snWxhi9qVaoo0pBQ130_head.
- NP502625.RAp3rPopBruIBrpwr-VnEU1knGul2snWxhi9qVaoo0pBQ130_assertion description "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502625.RAp3rPopBruIBrpwr-VnEU1knGul2snWxhi9qVaoo0pBQ130_provenance.
- NP502625.RAp3rPopBruIBrpwr-VnEU1knGul2snWxhi9qVaoo0pBQ130_assertion evidence source_evidence_literature NP502625.RAp3rPopBruIBrpwr-VnEU1knGul2snWxhi9qVaoo0pBQ130_provenance.
- NP502625.RAp3rPopBruIBrpwr-VnEU1knGul2snWxhi9qVaoo0pBQ130_assertion SIO_000772 16000300 NP502625.RAp3rPopBruIBrpwr-VnEU1knGul2snWxhi9qVaoo0pBQ130_provenance.
- NP502625.RAp3rPopBruIBrpwr-VnEU1knGul2snWxhi9qVaoo0pBQ130_assertion wasDerivedFrom befree-2016 NP502625.RAp3rPopBruIBrpwr-VnEU1knGul2snWxhi9qVaoo0pBQ130_provenance.
- NP502625.RAp3rPopBruIBrpwr-VnEU1knGul2snWxhi9qVaoo0pBQ130_assertion wasGeneratedBy ECO_0000203 NP502625.RAp3rPopBruIBrpwr-VnEU1knGul2snWxhi9qVaoo0pBQ130_provenance.