Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_assertion> ?p ?o ?g. }
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- NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_assertion type Assertion NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_head.
- NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_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." NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_provenance.
- NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_assertion evidence source_evidence_literature NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_provenance.
- NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_assertion SIO_000772 19211713 NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_provenance.
- NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_assertion wasDerivedFrom befree-2016 NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_provenance.
- NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_assertion wasGeneratedBy ECO_0000203 NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_provenance.