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- source_evidence_literature type ECO_0000212 NP270449.RAd0ieXGJ78m_zrGcO9ruCYfPVelNqmmbWmOluiOzJlc8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP270449.RAd0ieXGJ78m_zrGcO9ruCYfPVelNqmmbWmOluiOzJlc8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP270449.RAd0ieXGJ78m_zrGcO9ruCYfPVelNqmmbWmOluiOzJlc8130_provenance.
- NP270449.RAd0ieXGJ78m_zrGcO9ruCYfPVelNqmmbWmOluiOzJlc8130_assertion description "[Although it has recently been shown that ?97�% of all adult GCT harbor a novel somatic missense mutation in the FOXL2 gene, given its almost universal presence, it does not explain differences in tumor stage and/or recurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP270449.RAd0ieXGJ78m_zrGcO9ruCYfPVelNqmmbWmOluiOzJlc8130_provenance.
- NP270449.RAd0ieXGJ78m_zrGcO9ruCYfPVelNqmmbWmOluiOzJlc8130_assertion evidence source_evidence_literature NP270449.RAd0ieXGJ78m_zrGcO9ruCYfPVelNqmmbWmOluiOzJlc8130_provenance.
- NP270449.RAd0ieXGJ78m_zrGcO9ruCYfPVelNqmmbWmOluiOzJlc8130_assertion SIO_000772 23674259 NP270449.RAd0ieXGJ78m_zrGcO9ruCYfPVelNqmmbWmOluiOzJlc8130_provenance.
- NP270449.RAd0ieXGJ78m_zrGcO9ruCYfPVelNqmmbWmOluiOzJlc8130_assertion wasDerivedFrom befree-20150227 NP270449.RAd0ieXGJ78m_zrGcO9ruCYfPVelNqmmbWmOluiOzJlc8130_provenance.
- NP270449.RAd0ieXGJ78m_zrGcO9ruCYfPVelNqmmbWmOluiOzJlc8130_assertion wasGeneratedBy ECO_0000203 NP270449.RAd0ieXGJ78m_zrGcO9ruCYfPVelNqmmbWmOluiOzJlc8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP270449.RAd0ieXGJ78m_zrGcO9ruCYfPVelNqmmbWmOluiOzJlc8130_provenance.