Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_provenance.
- NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_provenance.
- NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_assertion evidence source_evidence_literature NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_provenance.
- NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_assertion SIO_000772 21862621 NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_provenance.
- NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_assertion wasDerivedFrom befree-2016 NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_provenance.
- NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_assertion wasGeneratedBy ECO_0000203 NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_provenance.
- befree-2016 importedOn "2016-02-19" NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_provenance.