Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP212015.RAZ10RoJfU6ksp0mJRvyk81Xev0HP4ocmH_-qCDj2LhDI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212015.RAZ10RoJfU6ksp0mJRvyk81Xev0HP4ocmH_-qCDj2LhDI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212015.RAZ10RoJfU6ksp0mJRvyk81Xev0HP4ocmH_-qCDj2LhDI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212015.RAZ10RoJfU6ksp0mJRvyk81Xev0HP4ocmH_-qCDj2LhDI130_provenance.
- NP212015.RAZ10RoJfU6ksp0mJRvyk81Xev0HP4ocmH_-qCDj2LhDI130_assertion description "[It is concluded that MECT1-MAML2 gene fusion is a highly specific genetic alteration in MEC with predominance in low-grade and intermediate-grade tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212015.RAZ10RoJfU6ksp0mJRvyk81Xev0HP4ocmH_-qCDj2LhDI130_provenance.
- NP212015.RAZ10RoJfU6ksp0mJRvyk81Xev0HP4ocmH_-qCDj2LhDI130_assertion evidence source_evidence_literature NP212015.RAZ10RoJfU6ksp0mJRvyk81Xev0HP4ocmH_-qCDj2LhDI130_provenance.
- NP212015.RAZ10RoJfU6ksp0mJRvyk81Xev0HP4ocmH_-qCDj2LhDI130_assertion SIO_000772 22847156 NP212015.RAZ10RoJfU6ksp0mJRvyk81Xev0HP4ocmH_-qCDj2LhDI130_provenance.
- NP212015.RAZ10RoJfU6ksp0mJRvyk81Xev0HP4ocmH_-qCDj2LhDI130_assertion wasDerivedFrom befree-20140225 NP212015.RAZ10RoJfU6ksp0mJRvyk81Xev0HP4ocmH_-qCDj2LhDI130_provenance.
- NP212015.RAZ10RoJfU6ksp0mJRvyk81Xev0HP4ocmH_-qCDj2LhDI130_assertion wasGeneratedBy ECO_0000203 NP212015.RAZ10RoJfU6ksp0mJRvyk81Xev0HP4ocmH_-qCDj2LhDI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212015.RAZ10RoJfU6ksp0mJRvyk81Xev0HP4ocmH_-qCDj2LhDI130_provenance.