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- source_evidence_literature type ECO_0000212 NP166315.RAMGePLaqON3pJ8B3yn3aAOi70DEbNEYF3oArak9nCbGg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP166315.RAMGePLaqON3pJ8B3yn3aAOi70DEbNEYF3oArak9nCbGg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP166315.RAMGePLaqON3pJ8B3yn3aAOi70DEbNEYF3oArak9nCbGg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP166315.RAMGePLaqON3pJ8B3yn3aAOi70DEbNEYF3oArak9nCbGg130_provenance.
- NP166315.RAMGePLaqON3pJ8B3yn3aAOi70DEbNEYF3oArak9nCbGg130_assertion wasGeneratedBy ECO_0000203 NP166315.RAMGePLaqON3pJ8B3yn3aAOi70DEbNEYF3oArak9nCbGg130_provenance.
- NP166315.RAMGePLaqON3pJ8B3yn3aAOi70DEbNEYF3oArak9nCbGg130_assertion wasDerivedFrom gad-20150221 NP166315.RAMGePLaqON3pJ8B3yn3aAOi70DEbNEYF3oArak9nCbGg130_provenance.
- NP166315.RAMGePLaqON3pJ8B3yn3aAOi70DEbNEYF3oArak9nCbGg130_assertion SIO_000772 20198651 NP166315.RAMGePLaqON3pJ8B3yn3aAOi70DEbNEYF3oArak9nCbGg130_provenance.
- NP166315.RAMGePLaqON3pJ8B3yn3aAOi70DEbNEYF3oArak9nCbGg130_assertion evidence source_evidence_literature NP166315.RAMGePLaqON3pJ8B3yn3aAOi70DEbNEYF3oArak9nCbGg130_provenance.
- NP166315.RAMGePLaqON3pJ8B3yn3aAOi70DEbNEYF3oArak9nCbGg130_assertion description "[Our data indicate that the FOXL2 codon 134 mutation occurs exclusively in GCT and thecoma, and suggest the possibility that the development of most GCTs and a fraction of thecomas may be dependent on this mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP166315.RAMGePLaqON3pJ8B3yn3aAOi70DEbNEYF3oArak9nCbGg130_provenance.