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- source_evidence_literature type ECO_0000212 NP109964.RAqp4_4gGmESiWQEdHpaXkd69JCMLnJ65KLi1jcQL3rwA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP109964.RAqp4_4gGmESiWQEdHpaXkd69JCMLnJ65KLi1jcQL3rwA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP109964.RAqp4_4gGmESiWQEdHpaXkd69JCMLnJ65KLi1jcQL3rwA130_provenance.
- NP109964.RAqp4_4gGmESiWQEdHpaXkd69JCMLnJ65KLi1jcQL3rwA130_assertion description "[Our findings indicate a reduced NMSC risk in relation to XPD Asp312Asn and Lys751Gln variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP109964.RAqp4_4gGmESiWQEdHpaXkd69JCMLnJ65KLi1jcQL3rwA130_provenance.
- NP109964.RAqp4_4gGmESiWQEdHpaXkd69JCMLnJ65KLi1jcQL3rwA130_assertion evidence source_evidence_literature NP109964.RAqp4_4gGmESiWQEdHpaXkd69JCMLnJ65KLi1jcQL3rwA130_provenance.
- NP109964.RAqp4_4gGmESiWQEdHpaXkd69JCMLnJ65KLi1jcQL3rwA130_assertion SIO_000772 17687452 NP109964.RAqp4_4gGmESiWQEdHpaXkd69JCMLnJ65KLi1jcQL3rwA130_provenance.
- NP109964.RAqp4_4gGmESiWQEdHpaXkd69JCMLnJ65KLi1jcQL3rwA130_assertion wasDerivedFrom gad-20150221 NP109964.RAqp4_4gGmESiWQEdHpaXkd69JCMLnJ65KLi1jcQL3rwA130_provenance.
- NP109964.RAqp4_4gGmESiWQEdHpaXkd69JCMLnJ65KLi1jcQL3rwA130_assertion wasGeneratedBy ECO_0000203 NP109964.RAqp4_4gGmESiWQEdHpaXkd69JCMLnJ65KLi1jcQL3rwA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP109964.RAqp4_4gGmESiWQEdHpaXkd69JCMLnJ65KLi1jcQL3rwA130_provenance.