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- source_evidence_literature type ECO_0000212 NP454822.RAXHi_V86fVKdIG0HADkodc-FJRr0-RNwFn_mKKLwkj7U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP454822.RAXHi_V86fVKdIG0HADkodc-FJRr0-RNwFn_mKKLwkj7U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP454822.RAXHi_V86fVKdIG0HADkodc-FJRr0-RNwFn_mKKLwkj7U130_provenance.
- NP454822.RAXHi_V86fVKdIG0HADkodc-FJRr0-RNwFn_mKKLwkj7U130_assertion description "[In the group of patients with AOD, those who were positive for DRB1*16 specificity have a statistically significant chance to develop EN, as opposed to those who are positive for DRB1*15 specificity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP454822.RAXHi_V86fVKdIG0HADkodc-FJRr0-RNwFn_mKKLwkj7U130_provenance.
- NP454822.RAXHi_V86fVKdIG0HADkodc-FJRr0-RNwFn_mKKLwkj7U130_assertion evidence source_evidence_literature NP454822.RAXHi_V86fVKdIG0HADkodc-FJRr0-RNwFn_mKKLwkj7U130_provenance.
- NP454822.RAXHi_V86fVKdIG0HADkodc-FJRr0-RNwFn_mKKLwkj7U130_assertion SIO_000772 17767551 NP454822.RAXHi_V86fVKdIG0HADkodc-FJRr0-RNwFn_mKKLwkj7U130_provenance.
- NP454822.RAXHi_V86fVKdIG0HADkodc-FJRr0-RNwFn_mKKLwkj7U130_assertion wasDerivedFrom befree-20150227 NP454822.RAXHi_V86fVKdIG0HADkodc-FJRr0-RNwFn_mKKLwkj7U130_provenance.
- NP454822.RAXHi_V86fVKdIG0HADkodc-FJRr0-RNwFn_mKKLwkj7U130_assertion wasGeneratedBy ECO_0000203 NP454822.RAXHi_V86fVKdIG0HADkodc-FJRr0-RNwFn_mKKLwkj7U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP454822.RAXHi_V86fVKdIG0HADkodc-FJRr0-RNwFn_mKKLwkj7U130_provenance.