Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP885899.RABUFSn3LdSXRlnx1EU2bd6ZeD2Np6OI1wGi23lTSFPEM130_assertion> ?p ?o ?g. }
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- NP885899.RABUFSn3LdSXRlnx1EU2bd6ZeD2Np6OI1wGi23lTSFPEM130_assertion type Assertion NP885899.RABUFSn3LdSXRlnx1EU2bd6ZeD2Np6OI1wGi23lTSFPEM130_head.
- NP885899.RABUFSn3LdSXRlnx1EU2bd6ZeD2Np6OI1wGi23lTSFPEM130_assertion description "[In addition, mutations in another member of the claudin family, CLDN19, were identified in a subset of patients with FHHNC with visual impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP885899.RABUFSn3LdSXRlnx1EU2bd6ZeD2Np6OI1wGi23lTSFPEM130_provenance.
- NP885899.RABUFSn3LdSXRlnx1EU2bd6ZeD2Np6OI1wGi23lTSFPEM130_assertion evidence source_evidence_literature NP885899.RABUFSn3LdSXRlnx1EU2bd6ZeD2Np6OI1wGi23lTSFPEM130_provenance.
- NP885899.RABUFSn3LdSXRlnx1EU2bd6ZeD2Np6OI1wGi23lTSFPEM130_assertion SIO_000772 21186073 NP885899.RABUFSn3LdSXRlnx1EU2bd6ZeD2Np6OI1wGi23lTSFPEM130_provenance.
- NP885899.RABUFSn3LdSXRlnx1EU2bd6ZeD2Np6OI1wGi23lTSFPEM130_assertion wasDerivedFrom befree-20140225 NP885899.RABUFSn3LdSXRlnx1EU2bd6ZeD2Np6OI1wGi23lTSFPEM130_provenance.
- NP885899.RABUFSn3LdSXRlnx1EU2bd6ZeD2Np6OI1wGi23lTSFPEM130_assertion wasGeneratedBy ECO_0000203 NP885899.RABUFSn3LdSXRlnx1EU2bd6ZeD2Np6OI1wGi23lTSFPEM130_provenance.