Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP886239.RArrwxiONdZx6Tez7bL4-ebzBZ7xnVjID7PsUwO6pGF-w130_assertion> ?p ?o ?g. }
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- NP886239.RArrwxiONdZx6Tez7bL4-ebzBZ7xnVjID7PsUwO6pGF-w130_assertion type Assertion NP886239.RArrwxiONdZx6Tez7bL4-ebzBZ7xnVjID7PsUwO6pGF-w130_head.
- NP886239.RArrwxiONdZx6Tez7bL4-ebzBZ7xnVjID7PsUwO6pGF-w130_assertion wasGeneratedBy ECO_0000203 NP886239.RArrwxiONdZx6Tez7bL4-ebzBZ7xnVjID7PsUwO6pGF-w130_provenance.
- NP886239.RArrwxiONdZx6Tez7bL4-ebzBZ7xnVjID7PsUwO6pGF-w130_assertion wasDerivedFrom befree-20150227 NP886239.RArrwxiONdZx6Tez7bL4-ebzBZ7xnVjID7PsUwO6pGF-w130_provenance.
- NP886239.RArrwxiONdZx6Tez7bL4-ebzBZ7xnVjID7PsUwO6pGF-w130_assertion SIO_000772 17216245 NP886239.RArrwxiONdZx6Tez7bL4-ebzBZ7xnVjID7PsUwO6pGF-w130_provenance.
- NP886239.RArrwxiONdZx6Tez7bL4-ebzBZ7xnVjID7PsUwO6pGF-w130_assertion evidence source_evidence_literature NP886239.RArrwxiONdZx6Tez7bL4-ebzBZ7xnVjID7PsUwO6pGF-w130_provenance.
- NP886239.RArrwxiONdZx6Tez7bL4-ebzBZ7xnVjID7PsUwO6pGF-w130_assertion description "[Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886239.RArrwxiONdZx6Tez7bL4-ebzBZ7xnVjID7PsUwO6pGF-w130_provenance.