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- NP530555.RAO-Cx2KYU3YsnUo1-JYbabij2QIuVUFPgJNB-WEmxJPo130_assertion type Assertion NP530555.RAO-Cx2KYU3YsnUo1-JYbabij2QIuVUFPgJNB-WEmxJPo130_head.
- NP530555.RAO-Cx2KYU3YsnUo1-JYbabij2QIuVUFPgJNB-WEmxJPo130_assertion wasGeneratedBy ECO_0000203 NP530555.RAO-Cx2KYU3YsnUo1-JYbabij2QIuVUFPgJNB-WEmxJPo130_provenance.
- NP530555.RAO-Cx2KYU3YsnUo1-JYbabij2QIuVUFPgJNB-WEmxJPo130_assertion wasDerivedFrom befree-20150227 NP530555.RAO-Cx2KYU3YsnUo1-JYbabij2QIuVUFPgJNB-WEmxJPo130_provenance.
- NP530555.RAO-Cx2KYU3YsnUo1-JYbabij2QIuVUFPgJNB-WEmxJPo130_assertion SIO_000772 21236492 NP530555.RAO-Cx2KYU3YsnUo1-JYbabij2QIuVUFPgJNB-WEmxJPo130_provenance.
- NP530555.RAO-Cx2KYU3YsnUo1-JYbabij2QIuVUFPgJNB-WEmxJPo130_assertion evidence source_evidence_literature NP530555.RAO-Cx2KYU3YsnUo1-JYbabij2QIuVUFPgJNB-WEmxJPo130_provenance.
- NP530555.RAO-Cx2KYU3YsnUo1-JYbabij2QIuVUFPgJNB-WEmxJPo130_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." NP530555.RAO-Cx2KYU3YsnUo1-JYbabij2QIuVUFPgJNB-WEmxJPo130_provenance.