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- NP680790.RATLUY5mNn7HU0sbDat_uy8iVwyQKy6klTaZhRnmIJhXM130_assertion type Assertion NP680790.RATLUY5mNn7HU0sbDat_uy8iVwyQKy6klTaZhRnmIJhXM130_head.
- NP680790.RATLUY5mNn7HU0sbDat_uy8iVwyQKy6klTaZhRnmIJhXM130_assertion wasGeneratedBy ECO_0000203 NP680790.RATLUY5mNn7HU0sbDat_uy8iVwyQKy6klTaZhRnmIJhXM130_provenance.
- NP680790.RATLUY5mNn7HU0sbDat_uy8iVwyQKy6klTaZhRnmIJhXM130_assertion wasDerivedFrom befree-20140225 NP680790.RATLUY5mNn7HU0sbDat_uy8iVwyQKy6klTaZhRnmIJhXM130_provenance.
- NP680790.RATLUY5mNn7HU0sbDat_uy8iVwyQKy6klTaZhRnmIJhXM130_assertion SIO_000772 17943323 NP680790.RATLUY5mNn7HU0sbDat_uy8iVwyQKy6klTaZhRnmIJhXM130_provenance.
- NP680790.RATLUY5mNn7HU0sbDat_uy8iVwyQKy6klTaZhRnmIJhXM130_assertion evidence source_evidence_literature NP680790.RATLUY5mNn7HU0sbDat_uy8iVwyQKy6klTaZhRnmIJhXM130_provenance.
- NP680790.RATLUY5mNn7HU0sbDat_uy8iVwyQKy6klTaZhRnmIJhXM130_assertion description "[Recently, mutations in the LAMB2 gene encoding laminin beta2 were described as the cause of Pierson syndrome, which is characterized by CNS and a complex ocular maldevelopment with microcoria as the most prominent clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP680790.RATLUY5mNn7HU0sbDat_uy8iVwyQKy6klTaZhRnmIJhXM130_provenance.