Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP744117.RAsUf4R8jdqSSBgTPgCWYHcbl4G4DsomrG4LYVSeevGco130_assertion> ?p ?o ?g. }
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- NP744117.RAsUf4R8jdqSSBgTPgCWYHcbl4G4DsomrG4LYVSeevGco130_assertion type Assertion NP744117.RAsUf4R8jdqSSBgTPgCWYHcbl4G4DsomrG4LYVSeevGco130_head.
- NP744117.RAsUf4R8jdqSSBgTPgCWYHcbl4G4DsomrG4LYVSeevGco130_assertion description "[Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP744117.RAsUf4R8jdqSSBgTPgCWYHcbl4G4DsomrG4LYVSeevGco130_provenance.
- NP744117.RAsUf4R8jdqSSBgTPgCWYHcbl4G4DsomrG4LYVSeevGco130_assertion evidence source_evidence_literature NP744117.RAsUf4R8jdqSSBgTPgCWYHcbl4G4DsomrG4LYVSeevGco130_provenance.
- NP744117.RAsUf4R8jdqSSBgTPgCWYHcbl4G4DsomrG4LYVSeevGco130_assertion SIO_000772 19508969 NP744117.RAsUf4R8jdqSSBgTPgCWYHcbl4G4DsomrG4LYVSeevGco130_provenance.
- NP744117.RAsUf4R8jdqSSBgTPgCWYHcbl4G4DsomrG4LYVSeevGco130_assertion wasDerivedFrom befree-2016 NP744117.RAsUf4R8jdqSSBgTPgCWYHcbl4G4DsomrG4LYVSeevGco130_provenance.
- NP744117.RAsUf4R8jdqSSBgTPgCWYHcbl4G4DsomrG4LYVSeevGco130_assertion wasGeneratedBy ECO_0000203 NP744117.RAsUf4R8jdqSSBgTPgCWYHcbl4G4DsomrG4LYVSeevGco130_provenance.