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- source_evidence_literature type ECO_0000212 NP275762.RAdQUcF0vWSxSofkmgNunZt0ryNlTZKCEAW_kn1El5K1A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP275762.RAdQUcF0vWSxSofkmgNunZt0ryNlTZKCEAW_kn1El5K1A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP275762.RAdQUcF0vWSxSofkmgNunZt0ryNlTZKCEAW_kn1El5K1A130_provenance.
- NP275762.RAdQUcF0vWSxSofkmgNunZt0ryNlTZKCEAW_kn1El5K1A130_assertion description "[The association of the rare C4B3 variant with microangiopathy suggests a genetic component of its aetiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP275762.RAdQUcF0vWSxSofkmgNunZt0ryNlTZKCEAW_kn1El5K1A130_provenance.
- NP275762.RAdQUcF0vWSxSofkmgNunZt0ryNlTZKCEAW_kn1El5K1A130_assertion evidence source_evidence_literature NP275762.RAdQUcF0vWSxSofkmgNunZt0ryNlTZKCEAW_kn1El5K1A130_provenance.
- NP275762.RAdQUcF0vWSxSofkmgNunZt0ryNlTZKCEAW_kn1El5K1A130_assertion SIO_000772 3926068 NP275762.RAdQUcF0vWSxSofkmgNunZt0ryNlTZKCEAW_kn1El5K1A130_provenance.
- NP275762.RAdQUcF0vWSxSofkmgNunZt0ryNlTZKCEAW_kn1El5K1A130_assertion wasDerivedFrom befree-20150227 NP275762.RAdQUcF0vWSxSofkmgNunZt0ryNlTZKCEAW_kn1El5K1A130_provenance.
- NP275762.RAdQUcF0vWSxSofkmgNunZt0ryNlTZKCEAW_kn1El5K1A130_assertion wasGeneratedBy ECO_0000203 NP275762.RAdQUcF0vWSxSofkmgNunZt0ryNlTZKCEAW_kn1El5K1A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP275762.RAdQUcF0vWSxSofkmgNunZt0ryNlTZKCEAW_kn1El5K1A130_provenance.