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- NP369786.RAVmEsReBFacQrMScm67pUyiErOzNZVFY3z0cd6NZuQc8130_assertion type Assertion NP369786.RAVmEsReBFacQrMScm67pUyiErOzNZVFY3z0cd6NZuQc8130_head.
- NP369786.RAVmEsReBFacQrMScm67pUyiErOzNZVFY3z0cd6NZuQc8130_assertion wasGeneratedBy ECO_0000203 NP369786.RAVmEsReBFacQrMScm67pUyiErOzNZVFY3z0cd6NZuQc8130_provenance.
- NP369786.RAVmEsReBFacQrMScm67pUyiErOzNZVFY3z0cd6NZuQc8130_assertion wasDerivedFrom befree-20140225 NP369786.RAVmEsReBFacQrMScm67pUyiErOzNZVFY3z0cd6NZuQc8130_provenance.
- NP369786.RAVmEsReBFacQrMScm67pUyiErOzNZVFY3z0cd6NZuQc8130_assertion SIO_000772 21236492 NP369786.RAVmEsReBFacQrMScm67pUyiErOzNZVFY3z0cd6NZuQc8130_provenance.
- NP369786.RAVmEsReBFacQrMScm67pUyiErOzNZVFY3z0cd6NZuQc8130_assertion evidence source_evidence_literature NP369786.RAVmEsReBFacQrMScm67pUyiErOzNZVFY3z0cd6NZuQc8130_provenance.
- NP369786.RAVmEsReBFacQrMScm67pUyiErOzNZVFY3z0cd6NZuQc8130_assertion description "[To describe a novel laminin β-2 (LAMB2) mutation associated with nephrotic syndrome and severe retinal disease without microcoria in a large, multigenerational family with Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP369786.RAVmEsReBFacQrMScm67pUyiErOzNZVFY3z0cd6NZuQc8130_provenance.