Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP270378.RAEkC4vYzaVbo9Tto9rl4iujnoS0M1NvPT5h3Hw5H0Eps130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP270378.RAEkC4vYzaVbo9Tto9rl4iujnoS0M1NvPT5h3Hw5H0Eps130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP270378.RAEkC4vYzaVbo9Tto9rl4iujnoS0M1NvPT5h3Hw5H0Eps130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP270378.RAEkC4vYzaVbo9Tto9rl4iujnoS0M1NvPT5h3Hw5H0Eps130_provenance.
- befree-20150227 importedOn "2015-02-27" NP270378.RAEkC4vYzaVbo9Tto9rl4iujnoS0M1NvPT5h3Hw5H0Eps130_provenance.
- NP270378.RAEkC4vYzaVbo9Tto9rl4iujnoS0M1NvPT5h3Hw5H0Eps130_assertion wasGeneratedBy ECO_0000203 NP270378.RAEkC4vYzaVbo9Tto9rl4iujnoS0M1NvPT5h3Hw5H0Eps130_provenance.
- NP270378.RAEkC4vYzaVbo9Tto9rl4iujnoS0M1NvPT5h3Hw5H0Eps130_assertion wasDerivedFrom befree-20150227 NP270378.RAEkC4vYzaVbo9Tto9rl4iujnoS0M1NvPT5h3Hw5H0Eps130_provenance.
- NP270378.RAEkC4vYzaVbo9Tto9rl4iujnoS0M1NvPT5h3Hw5H0Eps130_assertion SIO_000772 20198651 NP270378.RAEkC4vYzaVbo9Tto9rl4iujnoS0M1NvPT5h3Hw5H0Eps130_provenance.
- NP270378.RAEkC4vYzaVbo9Tto9rl4iujnoS0M1NvPT5h3Hw5H0Eps130_assertion evidence source_evidence_literature NP270378.RAEkC4vYzaVbo9Tto9rl4iujnoS0M1NvPT5h3Hw5H0Eps130_provenance.
- NP270378.RAEkC4vYzaVbo9Tto9rl4iujnoS0M1NvPT5h3Hw5H0Eps130_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." NP270378.RAEkC4vYzaVbo9Tto9rl4iujnoS0M1NvPT5h3Hw5H0Eps130_provenance.