Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP720059.RAmB6EzwVAqOax7PJi3qKl98bdSa4OUlx5X_-fQLBSANQ130_assertion> ?p ?o ?g. }
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- NP720059.RAmB6EzwVAqOax7PJi3qKl98bdSa4OUlx5X_-fQLBSANQ130_assertion type Assertion NP720059.RAmB6EzwVAqOax7PJi3qKl98bdSa4OUlx5X_-fQLBSANQ130_head.
- NP720059.RAmB6EzwVAqOax7PJi3qKl98bdSa4OUlx5X_-fQLBSANQ130_assertion description "[Meckel-Gruber syndrome type 3 (MKS3; OMIM 607361) is a severe autosomal recessive disorder characterized by bilateral polycystic kidney disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720059.RAmB6EzwVAqOax7PJi3qKl98bdSa4OUlx5X_-fQLBSANQ130_provenance.
- NP720059.RAmB6EzwVAqOax7PJi3qKl98bdSa4OUlx5X_-fQLBSANQ130_assertion evidence source_evidence_literature NP720059.RAmB6EzwVAqOax7PJi3qKl98bdSa4OUlx5X_-fQLBSANQ130_provenance.
- NP720059.RAmB6EzwVAqOax7PJi3qKl98bdSa4OUlx5X_-fQLBSANQ130_assertion SIO_000772 19211713 NP720059.RAmB6EzwVAqOax7PJi3qKl98bdSa4OUlx5X_-fQLBSANQ130_provenance.
- NP720059.RAmB6EzwVAqOax7PJi3qKl98bdSa4OUlx5X_-fQLBSANQ130_assertion wasDerivedFrom befree-2016 NP720059.RAmB6EzwVAqOax7PJi3qKl98bdSa4OUlx5X_-fQLBSANQ130_provenance.
- NP720059.RAmB6EzwVAqOax7PJi3qKl98bdSa4OUlx5X_-fQLBSANQ130_assertion wasGeneratedBy ECO_0000203 NP720059.RAmB6EzwVAqOax7PJi3qKl98bdSa4OUlx5X_-fQLBSANQ130_provenance.