Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP386618.RAcHL4HG2UAgc2AliuleDgf4hN0S5EOMjPYUugXoS4CbA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP386618.RAcHL4HG2UAgc2AliuleDgf4hN0S5EOMjPYUugXoS4CbA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP386618.RAcHL4HG2UAgc2AliuleDgf4hN0S5EOMjPYUugXoS4CbA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP386618.RAcHL4HG2UAgc2AliuleDgf4hN0S5EOMjPYUugXoS4CbA130_provenance.
- NP386618.RAcHL4HG2UAgc2AliuleDgf4hN0S5EOMjPYUugXoS4CbA130_assertion description "[Our findings support the notion that FGF9 is a key factor contributing to the cancer phenotype of OEAs carrying Wnt/beta-catenin pathway defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386618.RAcHL4HG2UAgc2AliuleDgf4hN0S5EOMjPYUugXoS4CbA130_provenance.
- NP386618.RAcHL4HG2UAgc2AliuleDgf4hN0S5EOMjPYUugXoS4CbA130_assertion evidence source_evidence_literature NP386618.RAcHL4HG2UAgc2AliuleDgf4hN0S5EOMjPYUugXoS4CbA130_provenance.
- NP386618.RAcHL4HG2UAgc2AliuleDgf4hN0S5EOMjPYUugXoS4CbA130_assertion SIO_000772 16452189 NP386618.RAcHL4HG2UAgc2AliuleDgf4hN0S5EOMjPYUugXoS4CbA130_provenance.
- NP386618.RAcHL4HG2UAgc2AliuleDgf4hN0S5EOMjPYUugXoS4CbA130_assertion wasDerivedFrom befree-20140225 NP386618.RAcHL4HG2UAgc2AliuleDgf4hN0S5EOMjPYUugXoS4CbA130_provenance.
- NP386618.RAcHL4HG2UAgc2AliuleDgf4hN0S5EOMjPYUugXoS4CbA130_assertion wasGeneratedBy ECO_0000203 NP386618.RAcHL4HG2UAgc2AliuleDgf4hN0S5EOMjPYUugXoS4CbA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP386618.RAcHL4HG2UAgc2AliuleDgf4hN0S5EOMjPYUugXoS4CbA130_provenance.