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- source_evidence_literature type ECO_0000212 NP968757.RAwN_3mSUh5Xnxtz0fcIYeusmGUSuorBuhsMdzdvmGIII130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP968757.RAwN_3mSUh5Xnxtz0fcIYeusmGUSuorBuhsMdzdvmGIII130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP968757.RAwN_3mSUh5Xnxtz0fcIYeusmGUSuorBuhsMdzdvmGIII130_provenance.
- NP968757.RAwN_3mSUh5Xnxtz0fcIYeusmGUSuorBuhsMdzdvmGIII130_assertion description "[The presence of I allele was associated with an increased risk of CD (OR 1.35) and the effect of I allele was consistent with a recessive genetic model (P<0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968757.RAwN_3mSUh5Xnxtz0fcIYeusmGUSuorBuhsMdzdvmGIII130_provenance.
- NP968757.RAwN_3mSUh5Xnxtz0fcIYeusmGUSuorBuhsMdzdvmGIII130_assertion evidence source_evidence_literature NP968757.RAwN_3mSUh5Xnxtz0fcIYeusmGUSuorBuhsMdzdvmGIII130_provenance.
- NP968757.RAwN_3mSUh5Xnxtz0fcIYeusmGUSuorBuhsMdzdvmGIII130_assertion SIO_000772 20823837 NP968757.RAwN_3mSUh5Xnxtz0fcIYeusmGUSuorBuhsMdzdvmGIII130_provenance.
- NP968757.RAwN_3mSUh5Xnxtz0fcIYeusmGUSuorBuhsMdzdvmGIII130_assertion wasDerivedFrom befree-20150227 NP968757.RAwN_3mSUh5Xnxtz0fcIYeusmGUSuorBuhsMdzdvmGIII130_provenance.
- NP968757.RAwN_3mSUh5Xnxtz0fcIYeusmGUSuorBuhsMdzdvmGIII130_assertion wasGeneratedBy ECO_0000203 NP968757.RAwN_3mSUh5Xnxtz0fcIYeusmGUSuorBuhsMdzdvmGIII130_provenance.
- befree-20150227 importedOn "2015-02-27" NP968757.RAwN_3mSUh5Xnxtz0fcIYeusmGUSuorBuhsMdzdvmGIII130_provenance.