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- NP724507.RAv19yawSXXh-u2vdrBd5CAlt4yBd6U3dRA8MxA3Zv1Yk130_assertion type Assertion NP724507.RAv19yawSXXh-u2vdrBd5CAlt4yBd6U3dRA8MxA3Zv1Yk130_head.
- NP724507.RAv19yawSXXh-u2vdrBd5CAlt4yBd6U3dRA8MxA3Zv1Yk130_assertion wasGeneratedBy ECO_0000203 NP724507.RAv19yawSXXh-u2vdrBd5CAlt4yBd6U3dRA8MxA3Zv1Yk130_provenance.
- NP724507.RAv19yawSXXh-u2vdrBd5CAlt4yBd6U3dRA8MxA3Zv1Yk130_assertion wasDerivedFrom befree-20140225 NP724507.RAv19yawSXXh-u2vdrBd5CAlt4yBd6U3dRA8MxA3Zv1Yk130_provenance.
- NP724507.RAv19yawSXXh-u2vdrBd5CAlt4yBd6U3dRA8MxA3Zv1Yk130_assertion SIO_000772 10973248 NP724507.RAv19yawSXXh-u2vdrBd5CAlt4yBd6U3dRA8MxA3Zv1Yk130_provenance.
- NP724507.RAv19yawSXXh-u2vdrBd5CAlt4yBd6U3dRA8MxA3Zv1Yk130_assertion evidence source_evidence_literature NP724507.RAv19yawSXXh-u2vdrBd5CAlt4yBd6U3dRA8MxA3Zv1Yk130_provenance.
- NP724507.RAv19yawSXXh-u2vdrBd5CAlt4yBd6U3dRA8MxA3Zv1Yk130_assertion description "[The molecular basis of the disorder is a homozygous 122-kb deletion of 11p14-15, which includes part of ABCC8 and overlaps with the locus for Usher syndrome type 1C and DFNB18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724507.RAv19yawSXXh-u2vdrBd5CAlt4yBd6U3dRA8MxA3Zv1Yk130_provenance.