Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_assertion> ?p ?o ?g. }
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- NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_assertion type Assertion NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_head.
- NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_assertion description "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_provenance.
- NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_assertion evidence source_evidence_literature NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_provenance.
- NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_assertion SIO_000772 16000300 NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_provenance.
- NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_assertion wasDerivedFrom befree-20150227 NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_provenance.
- NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_assertion wasGeneratedBy ECO_0000203 NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_provenance.