Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP958113.RAY4i4XPbcZ0DjV4jM2l0i7Ow8K1fJ9DNKzYBiVhJaFXQ130_assertion> ?p ?o ?g. }
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- NP958113.RAY4i4XPbcZ0DjV4jM2l0i7Ow8K1fJ9DNKzYBiVhJaFXQ130_assertion type Assertion NP958113.RAY4i4XPbcZ0DjV4jM2l0i7Ow8K1fJ9DNKzYBiVhJaFXQ130_head.
- NP958113.RAY4i4XPbcZ0DjV4jM2l0i7Ow8K1fJ9DNKzYBiVhJaFXQ130_assertion wasGeneratedBy ECO_0000203 NP958113.RAY4i4XPbcZ0DjV4jM2l0i7Ow8K1fJ9DNKzYBiVhJaFXQ130_provenance.
- NP958113.RAY4i4XPbcZ0DjV4jM2l0i7Ow8K1fJ9DNKzYBiVhJaFXQ130_assertion wasDerivedFrom befree-20150227 NP958113.RAY4i4XPbcZ0DjV4jM2l0i7Ow8K1fJ9DNKzYBiVhJaFXQ130_provenance.
- NP958113.RAY4i4XPbcZ0DjV4jM2l0i7Ow8K1fJ9DNKzYBiVhJaFXQ130_assertion SIO_000772 21236492 NP958113.RAY4i4XPbcZ0DjV4jM2l0i7Ow8K1fJ9DNKzYBiVhJaFXQ130_provenance.
- NP958113.RAY4i4XPbcZ0DjV4jM2l0i7Ow8K1fJ9DNKzYBiVhJaFXQ130_assertion evidence source_evidence_literature NP958113.RAY4i4XPbcZ0DjV4jM2l0i7Ow8K1fJ9DNKzYBiVhJaFXQ130_provenance.
- NP958113.RAY4i4XPbcZ0DjV4jM2l0i7Ow8K1fJ9DNKzYBiVhJaFXQ130_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." NP958113.RAY4i4XPbcZ0DjV4jM2l0i7Ow8K1fJ9DNKzYBiVhJaFXQ130_provenance.