Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_provenance.
- NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_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." NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_provenance.
- NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_assertion evidence source_evidence_literature NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_provenance.
- NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_assertion SIO_000772 21862621 NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_provenance.
- NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_assertion wasDerivedFrom befree-20150227 NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_provenance.
- NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_assertion wasGeneratedBy ECO_0000203 NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_provenance.