Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP230115.RA9plBXyJNGminSPSFbvjcr9SbGAAro_BRDCmoJv_ax3Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP230115.RA9plBXyJNGminSPSFbvjcr9SbGAAro_BRDCmoJv_ax3Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP230115.RA9plBXyJNGminSPSFbvjcr9SbGAAro_BRDCmoJv_ax3Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP230115.RA9plBXyJNGminSPSFbvjcr9SbGAAro_BRDCmoJv_ax3Y130_provenance.
- NP230115.RA9plBXyJNGminSPSFbvjcr9SbGAAro_BRDCmoJv_ax3Y130_assertion description "[Fusion of the nucleoporin gene, NUP98, and the putative RNA helicase gene, DDX10, by inversion 11 (p15q22) chromosome translocation in a patient with etoposide-related myelodysplastic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230115.RA9plBXyJNGminSPSFbvjcr9SbGAAro_BRDCmoJv_ax3Y130_provenance.
- NP230115.RA9plBXyJNGminSPSFbvjcr9SbGAAro_BRDCmoJv_ax3Y130_assertion evidence source_evidence_literature NP230115.RA9plBXyJNGminSPSFbvjcr9SbGAAro_BRDCmoJv_ax3Y130_provenance.
- NP230115.RA9plBXyJNGminSPSFbvjcr9SbGAAro_BRDCmoJv_ax3Y130_assertion SIO_000772 10830185 NP230115.RA9plBXyJNGminSPSFbvjcr9SbGAAro_BRDCmoJv_ax3Y130_provenance.
- NP230115.RA9plBXyJNGminSPSFbvjcr9SbGAAro_BRDCmoJv_ax3Y130_assertion wasDerivedFrom befree-20140225 NP230115.RA9plBXyJNGminSPSFbvjcr9SbGAAro_BRDCmoJv_ax3Y130_provenance.
- NP230115.RA9plBXyJNGminSPSFbvjcr9SbGAAro_BRDCmoJv_ax3Y130_assertion wasGeneratedBy ECO_0000203 NP230115.RA9plBXyJNGminSPSFbvjcr9SbGAAro_BRDCmoJv_ax3Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP230115.RA9plBXyJNGminSPSFbvjcr9SbGAAro_BRDCmoJv_ax3Y130_provenance.