Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP597108.RA9_aPVi18sKITBblWMK7yxxNmprOdzgvlIRjDw3ZZEVQ130_assertion> ?p ?o ?g. }
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- NP597108.RA9_aPVi18sKITBblWMK7yxxNmprOdzgvlIRjDw3ZZEVQ130_assertion type Assertion NP597108.RA9_aPVi18sKITBblWMK7yxxNmprOdzgvlIRjDw3ZZEVQ130_head.
- NP597108.RA9_aPVi18sKITBblWMK7yxxNmprOdzgvlIRjDw3ZZEVQ130_assertion description "[ACE D allele frequency of the I/D polymorphism was associated with an increased risk of SSc, suggesting a genetic contribution to the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597108.RA9_aPVi18sKITBblWMK7yxxNmprOdzgvlIRjDw3ZZEVQ130_provenance.
- NP597108.RA9_aPVi18sKITBblWMK7yxxNmprOdzgvlIRjDw3ZZEVQ130_assertion evidence source_evidence_literature NP597108.RA9_aPVi18sKITBblWMK7yxxNmprOdzgvlIRjDw3ZZEVQ130_provenance.
- NP597108.RA9_aPVi18sKITBblWMK7yxxNmprOdzgvlIRjDw3ZZEVQ130_assertion SIO_000772 15016346 NP597108.RA9_aPVi18sKITBblWMK7yxxNmprOdzgvlIRjDw3ZZEVQ130_provenance.
- NP597108.RA9_aPVi18sKITBblWMK7yxxNmprOdzgvlIRjDw3ZZEVQ130_assertion wasDerivedFrom befree-20140225 NP597108.RA9_aPVi18sKITBblWMK7yxxNmprOdzgvlIRjDw3ZZEVQ130_provenance.
- NP597108.RA9_aPVi18sKITBblWMK7yxxNmprOdzgvlIRjDw3ZZEVQ130_assertion wasGeneratedBy ECO_0000203 NP597108.RA9_aPVi18sKITBblWMK7yxxNmprOdzgvlIRjDw3ZZEVQ130_provenance.