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- source_evidence_literature type ECO_0000212 NP529221.RA9HqYbSzjP6YfOxxR0Sa45FwVmnSTxxPLdNB84HEecFI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP529221.RA9HqYbSzjP6YfOxxR0Sa45FwVmnSTxxPLdNB84HEecFI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP529221.RA9HqYbSzjP6YfOxxR0Sa45FwVmnSTxxPLdNB84HEecFI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP529221.RA9HqYbSzjP6YfOxxR0Sa45FwVmnSTxxPLdNB84HEecFI130_provenance.
- NP529221.RA9HqYbSzjP6YfOxxR0Sa45FwVmnSTxxPLdNB84HEecFI130_assertion wasGeneratedBy ECO_0000203 NP529221.RA9HqYbSzjP6YfOxxR0Sa45FwVmnSTxxPLdNB84HEecFI130_provenance.
- NP529221.RA9HqYbSzjP6YfOxxR0Sa45FwVmnSTxxPLdNB84HEecFI130_assertion wasDerivedFrom befree-20150227 NP529221.RA9HqYbSzjP6YfOxxR0Sa45FwVmnSTxxPLdNB84HEecFI130_provenance.
- NP529221.RA9HqYbSzjP6YfOxxR0Sa45FwVmnSTxxPLdNB84HEecFI130_assertion SIO_000772 19785597 NP529221.RA9HqYbSzjP6YfOxxR0Sa45FwVmnSTxxPLdNB84HEecFI130_provenance.
- NP529221.RA9HqYbSzjP6YfOxxR0Sa45FwVmnSTxxPLdNB84HEecFI130_assertion evidence source_evidence_literature NP529221.RA9HqYbSzjP6YfOxxR0Sa45FwVmnSTxxPLdNB84HEecFI130_provenance.
- NP529221.RA9HqYbSzjP6YfOxxR0Sa45FwVmnSTxxPLdNB84HEecFI130_assertion description "[This observation suggests that coinheritance of mutations in KRT16 and FLG may aggravate the PC phenotype and that FLG could serve as a genetic modifier in PC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP529221.RA9HqYbSzjP6YfOxxR0Sa45FwVmnSTxxPLdNB84HEecFI130_provenance.