Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP456335.RA9M9ZDeyFhfIo1RrqtPVsiZfdclMG12Z_8lRwMCyysBQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP456335.RA9M9ZDeyFhfIo1RrqtPVsiZfdclMG12Z_8lRwMCyysBQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP456335.RA9M9ZDeyFhfIo1RrqtPVsiZfdclMG12Z_8lRwMCyysBQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP456335.RA9M9ZDeyFhfIo1RrqtPVsiZfdclMG12Z_8lRwMCyysBQ130_provenance.
- NP456335.RA9M9ZDeyFhfIo1RrqtPVsiZfdclMG12Z_8lRwMCyysBQ130_assertion description "[These results imply distinct molecular mechanisms for monosomy 7 and trisomy 8 MDS and implicate specific pathogenic pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP456335.RA9M9ZDeyFhfIo1RrqtPVsiZfdclMG12Z_8lRwMCyysBQ130_provenance.
- NP456335.RA9M9ZDeyFhfIo1RrqtPVsiZfdclMG12Z_8lRwMCyysBQ130_assertion evidence source_evidence_literature NP456335.RA9M9ZDeyFhfIo1RrqtPVsiZfdclMG12Z_8lRwMCyysBQ130_provenance.
- NP456335.RA9M9ZDeyFhfIo1RrqtPVsiZfdclMG12Z_8lRwMCyysBQ130_assertion SIO_000772 15315976 NP456335.RA9M9ZDeyFhfIo1RrqtPVsiZfdclMG12Z_8lRwMCyysBQ130_provenance.
- NP456335.RA9M9ZDeyFhfIo1RrqtPVsiZfdclMG12Z_8lRwMCyysBQ130_assertion wasDerivedFrom befree-2016 NP456335.RA9M9ZDeyFhfIo1RrqtPVsiZfdclMG12Z_8lRwMCyysBQ130_provenance.
- NP456335.RA9M9ZDeyFhfIo1RrqtPVsiZfdclMG12Z_8lRwMCyysBQ130_assertion wasGeneratedBy ECO_0000203 NP456335.RA9M9ZDeyFhfIo1RrqtPVsiZfdclMG12Z_8lRwMCyysBQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP456335.RA9M9ZDeyFhfIo1RrqtPVsiZfdclMG12Z_8lRwMCyysBQ130_provenance.