Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP780011.RAdxI_sb8DrA6K9yftOW-DzDv8F1EYGS9HmsOXtGZT90Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP780011.RAdxI_sb8DrA6K9yftOW-DzDv8F1EYGS9HmsOXtGZT90Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP780011.RAdxI_sb8DrA6K9yftOW-DzDv8F1EYGS9HmsOXtGZT90Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP780011.RAdxI_sb8DrA6K9yftOW-DzDv8F1EYGS9HmsOXtGZT90Q130_provenance.
- NP780011.RAdxI_sb8DrA6K9yftOW-DzDv8F1EYGS9HmsOXtGZT90Q130_assertion description "[A new FOXL2 gene mutation in a woman with premature ovarian failure and sporadic blepharophimosis-ptosis-epicanthus inversus syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP780011.RAdxI_sb8DrA6K9yftOW-DzDv8F1EYGS9HmsOXtGZT90Q130_provenance.
- NP780011.RAdxI_sb8DrA6K9yftOW-DzDv8F1EYGS9HmsOXtGZT90Q130_assertion evidence source_evidence_literature NP780011.RAdxI_sb8DrA6K9yftOW-DzDv8F1EYGS9HmsOXtGZT90Q130_provenance.
- NP780011.RAdxI_sb8DrA6K9yftOW-DzDv8F1EYGS9HmsOXtGZT90Q130_assertion SIO_000772 19969293 NP780011.RAdxI_sb8DrA6K9yftOW-DzDv8F1EYGS9HmsOXtGZT90Q130_provenance.
- NP780011.RAdxI_sb8DrA6K9yftOW-DzDv8F1EYGS9HmsOXtGZT90Q130_assertion wasDerivedFrom befree-2016 NP780011.RAdxI_sb8DrA6K9yftOW-DzDv8F1EYGS9HmsOXtGZT90Q130_provenance.
- NP780011.RAdxI_sb8DrA6K9yftOW-DzDv8F1EYGS9HmsOXtGZT90Q130_assertion wasGeneratedBy ECO_0000203 NP780011.RAdxI_sb8DrA6K9yftOW-DzDv8F1EYGS9HmsOXtGZT90Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP780011.RAdxI_sb8DrA6K9yftOW-DzDv8F1EYGS9HmsOXtGZT90Q130_provenance.