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- NP549738.RAltJpOHu31NrYwaoocjPUojoZihUFr8EJkPbKC5bAVjQ130_assertion type Assertion NP549738.RAltJpOHu31NrYwaoocjPUojoZihUFr8EJkPbKC5bAVjQ130_head.
- NP549738.RAltJpOHu31NrYwaoocjPUojoZihUFr8EJkPbKC5bAVjQ130_assertion wasGeneratedBy ECO_0000203 NP549738.RAltJpOHu31NrYwaoocjPUojoZihUFr8EJkPbKC5bAVjQ130_provenance.
- NP549738.RAltJpOHu31NrYwaoocjPUojoZihUFr8EJkPbKC5bAVjQ130_assertion wasDerivedFrom befree-20140225 NP549738.RAltJpOHu31NrYwaoocjPUojoZihUFr8EJkPbKC5bAVjQ130_provenance.
- NP549738.RAltJpOHu31NrYwaoocjPUojoZihUFr8EJkPbKC5bAVjQ130_assertion SIO_000772 15735646 NP549738.RAltJpOHu31NrYwaoocjPUojoZihUFr8EJkPbKC5bAVjQ130_provenance.
- NP549738.RAltJpOHu31NrYwaoocjPUojoZihUFr8EJkPbKC5bAVjQ130_assertion evidence source_evidence_literature NP549738.RAltJpOHu31NrYwaoocjPUojoZihUFr8EJkPbKC5bAVjQ130_provenance.
- NP549738.RAltJpOHu31NrYwaoocjPUojoZihUFr8EJkPbKC5bAVjQ130_assertion description "[Autosomal dominant mutations in the gene encoding the basic helix-loop-helix transcription factor Twist1 are associated with limb and craniofacial defects in humans with Saethre-Chotzen syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549738.RAltJpOHu31NrYwaoocjPUojoZihUFr8EJkPbKC5bAVjQ130_provenance.