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- NP947448.RAA-5EQd_8nmlLGD7FVbUCx-Tq1y3sG2VcbordNpkK_iQ130_assertion type Assertion NP947448.RAA-5EQd_8nmlLGD7FVbUCx-Tq1y3sG2VcbordNpkK_iQ130_head.
- NP947448.RAA-5EQd_8nmlLGD7FVbUCx-Tq1y3sG2VcbordNpkK_iQ130_assertion description "[Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP947448.RAA-5EQd_8nmlLGD7FVbUCx-Tq1y3sG2VcbordNpkK_iQ130_provenance.
- NP947448.RAA-5EQd_8nmlLGD7FVbUCx-Tq1y3sG2VcbordNpkK_iQ130_assertion evidence source_evidence_literature NP947448.RAA-5EQd_8nmlLGD7FVbUCx-Tq1y3sG2VcbordNpkK_iQ130_provenance.
- NP947448.RAA-5EQd_8nmlLGD7FVbUCx-Tq1y3sG2VcbordNpkK_iQ130_assertion SIO_000772 22178368 NP947448.RAA-5EQd_8nmlLGD7FVbUCx-Tq1y3sG2VcbordNpkK_iQ130_provenance.
- NP947448.RAA-5EQd_8nmlLGD7FVbUCx-Tq1y3sG2VcbordNpkK_iQ130_assertion wasDerivedFrom befree-2016 NP947448.RAA-5EQd_8nmlLGD7FVbUCx-Tq1y3sG2VcbordNpkK_iQ130_provenance.
- NP947448.RAA-5EQd_8nmlLGD7FVbUCx-Tq1y3sG2VcbordNpkK_iQ130_assertion wasGeneratedBy ECO_0000203 NP947448.RAA-5EQd_8nmlLGD7FVbUCx-Tq1y3sG2VcbordNpkK_iQ130_provenance.