Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_provenance.