Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP832124.RAFTXv1VP189Z9IeskNEAvlFM0GNS49piAMdpn56pFjlM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP832124.RAFTXv1VP189Z9IeskNEAvlFM0GNS49piAMdpn56pFjlM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP832124.RAFTXv1VP189Z9IeskNEAvlFM0GNS49piAMdpn56pFjlM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP832124.RAFTXv1VP189Z9IeskNEAvlFM0GNS49piAMdpn56pFjlM130_provenance.
- NP832124.RAFTXv1VP189Z9IeskNEAvlFM0GNS49piAMdpn56pFjlM130_assertion description "[The MNNG-exposed Bloom syndrome (BS) B-lymphoblastoid cell population (BS-MNNG), when analyzed for aberrant genetic variations, showed an illegitimate rearrangement at the TCR-gamma gene and hypermethylation at the c-myb protooncogene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP832124.RAFTXv1VP189Z9IeskNEAvlFM0GNS49piAMdpn56pFjlM130_provenance.
- NP832124.RAFTXv1VP189Z9IeskNEAvlFM0GNS49piAMdpn56pFjlM130_assertion evidence source_evidence_literature NP832124.RAFTXv1VP189Z9IeskNEAvlFM0GNS49piAMdpn56pFjlM130_provenance.
- NP832124.RAFTXv1VP189Z9IeskNEAvlFM0GNS49piAMdpn56pFjlM130_assertion SIO_000772 9563641 NP832124.RAFTXv1VP189Z9IeskNEAvlFM0GNS49piAMdpn56pFjlM130_provenance.
- NP832124.RAFTXv1VP189Z9IeskNEAvlFM0GNS49piAMdpn56pFjlM130_assertion wasDerivedFrom befree-20150227 NP832124.RAFTXv1VP189Z9IeskNEAvlFM0GNS49piAMdpn56pFjlM130_provenance.
- NP832124.RAFTXv1VP189Z9IeskNEAvlFM0GNS49piAMdpn56pFjlM130_assertion wasGeneratedBy ECO_0000203 NP832124.RAFTXv1VP189Z9IeskNEAvlFM0GNS49piAMdpn56pFjlM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP832124.RAFTXv1VP189Z9IeskNEAvlFM0GNS49piAMdpn56pFjlM130_provenance.