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- NP843761.RAu59dN6WEigb5D2GJtDRjTjcWX2P5Ek_sD9mPY7i48Z8130_assertion type Assertion NP843761.RAu59dN6WEigb5D2GJtDRjTjcWX2P5Ek_sD9mPY7i48Z8130_head.
- NP843761.RAu59dN6WEigb5D2GJtDRjTjcWX2P5Ek_sD9mPY7i48Z8130_assertion wasGeneratedBy ECO_0000203 NP843761.RAu59dN6WEigb5D2GJtDRjTjcWX2P5Ek_sD9mPY7i48Z8130_provenance.
- NP843761.RAu59dN6WEigb5D2GJtDRjTjcWX2P5Ek_sD9mPY7i48Z8130_assertion wasDerivedFrom befree-20140225 NP843761.RAu59dN6WEigb5D2GJtDRjTjcWX2P5Ek_sD9mPY7i48Z8130_provenance.
- NP843761.RAu59dN6WEigb5D2GJtDRjTjcWX2P5Ek_sD9mPY7i48Z8130_assertion SIO_000772 23456818 NP843761.RAu59dN6WEigb5D2GJtDRjTjcWX2P5Ek_sD9mPY7i48Z8130_provenance.
- NP843761.RAu59dN6WEigb5D2GJtDRjTjcWX2P5Ek_sD9mPY7i48Z8130_assertion evidence source_evidence_literature NP843761.RAu59dN6WEigb5D2GJtDRjTjcWX2P5Ek_sD9mPY7i48Z8130_provenance.
- NP843761.RAu59dN6WEigb5D2GJtDRjTjcWX2P5Ek_sD9mPY7i48Z8130_assertion description "[Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP843761.RAu59dN6WEigb5D2GJtDRjTjcWX2P5Ek_sD9mPY7i48Z8130_provenance.