Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP935454.RAsxLHICvsm8aupsIfE8GfuFhwSil8xnaTGxsZuZTyYlY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP935454.RAsxLHICvsm8aupsIfE8GfuFhwSil8xnaTGxsZuZTyYlY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935454.RAsxLHICvsm8aupsIfE8GfuFhwSil8xnaTGxsZuZTyYlY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935454.RAsxLHICvsm8aupsIfE8GfuFhwSil8xnaTGxsZuZTyYlY130_provenance.
- NP935454.RAsxLHICvsm8aupsIfE8GfuFhwSil8xnaTGxsZuZTyYlY130_assertion description "[Our results show that BRAF mutation can also be present in CCS and support the proposed aberration of chromosomes 22 and 8 as a possibly useful nonrandom hallmark of EWSR1- CCS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935454.RAsxLHICvsm8aupsIfE8GfuFhwSil8xnaTGxsZuZTyYlY130_provenance.
- NP935454.RAsxLHICvsm8aupsIfE8GfuFhwSil8xnaTGxsZuZTyYlY130_assertion evidence source_evidence_literature NP935454.RAsxLHICvsm8aupsIfE8GfuFhwSil8xnaTGxsZuZTyYlY130_provenance.
- NP935454.RAsxLHICvsm8aupsIfE8GfuFhwSil8xnaTGxsZuZTyYlY130_assertion SIO_000772 22045652 NP935454.RAsxLHICvsm8aupsIfE8GfuFhwSil8xnaTGxsZuZTyYlY130_provenance.
- NP935454.RAsxLHICvsm8aupsIfE8GfuFhwSil8xnaTGxsZuZTyYlY130_assertion wasDerivedFrom befree-2016 NP935454.RAsxLHICvsm8aupsIfE8GfuFhwSil8xnaTGxsZuZTyYlY130_provenance.
- NP935454.RAsxLHICvsm8aupsIfE8GfuFhwSil8xnaTGxsZuZTyYlY130_assertion wasGeneratedBy ECO_0000203 NP935454.RAsxLHICvsm8aupsIfE8GfuFhwSil8xnaTGxsZuZTyYlY130_provenance.
- befree-2016 importedOn "2016-02-19" NP935454.RAsxLHICvsm8aupsIfE8GfuFhwSil8xnaTGxsZuZTyYlY130_provenance.