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- source_evidence_literature type ECO_0000212 NP163092.RAP5S_mw3BudNjFnNmmHJnz3dsU54IBsMsQzt_QTPyhxw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP163092.RAP5S_mw3BudNjFnNmmHJnz3dsU54IBsMsQzt_QTPyhxw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP163092.RAP5S_mw3BudNjFnNmmHJnz3dsU54IBsMsQzt_QTPyhxw130_provenance.
- NP163092.RAP5S_mw3BudNjFnNmmHJnz3dsU54IBsMsQzt_QTPyhxw130_assertion description "[Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163092.RAP5S_mw3BudNjFnNmmHJnz3dsU54IBsMsQzt_QTPyhxw130_provenance.
- NP163092.RAP5S_mw3BudNjFnNmmHJnz3dsU54IBsMsQzt_QTPyhxw130_assertion evidence source_evidence_literature NP163092.RAP5S_mw3BudNjFnNmmHJnz3dsU54IBsMsQzt_QTPyhxw130_provenance.
- NP163092.RAP5S_mw3BudNjFnNmmHJnz3dsU54IBsMsQzt_QTPyhxw130_assertion SIO_000772 20094846 NP163092.RAP5S_mw3BudNjFnNmmHJnz3dsU54IBsMsQzt_QTPyhxw130_provenance.
- NP163092.RAP5S_mw3BudNjFnNmmHJnz3dsU54IBsMsQzt_QTPyhxw130_assertion wasDerivedFrom gad-20150221 NP163092.RAP5S_mw3BudNjFnNmmHJnz3dsU54IBsMsQzt_QTPyhxw130_provenance.
- NP163092.RAP5S_mw3BudNjFnNmmHJnz3dsU54IBsMsQzt_QTPyhxw130_assertion wasGeneratedBy ECO_0000203 NP163092.RAP5S_mw3BudNjFnNmmHJnz3dsU54IBsMsQzt_QTPyhxw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP163092.RAP5S_mw3BudNjFnNmmHJnz3dsU54IBsMsQzt_QTPyhxw130_provenance.