Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1346353.RAKv72fJotrhNMbDFjXKPVFpE16f39z-ZFwVld_unwRTI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1346353.RAKv72fJotrhNMbDFjXKPVFpE16f39z-ZFwVld_unwRTI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1346353.RAKv72fJotrhNMbDFjXKPVFpE16f39z-ZFwVld_unwRTI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1346353.RAKv72fJotrhNMbDFjXKPVFpE16f39z-ZFwVld_unwRTI130_provenance.
- NP1346353.RAKv72fJotrhNMbDFjXKPVFpE16f39z-ZFwVld_unwRTI130_assertion description "[No rearrangements or deletions of the INK4d gene were observed in Southern blot analysis of selected cases of pediatric acute lymphoblastic leukemia (ALL) containing a variant (1;19)(q23;p13) translocation that lacks rearrangement of either E2A or PBX1, or in ALL cases containing homozygous or hemizygous deletions of the related genes, INK4a and INK4b.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1346353.RAKv72fJotrhNMbDFjXKPVFpE16f39z-ZFwVld_unwRTI130_provenance.
- NP1346353.RAKv72fJotrhNMbDFjXKPVFpE16f39z-ZFwVld_unwRTI130_assertion evidence source_evidence_literature NP1346353.RAKv72fJotrhNMbDFjXKPVFpE16f39z-ZFwVld_unwRTI130_provenance.
- NP1346353.RAKv72fJotrhNMbDFjXKPVFpE16f39z-ZFwVld_unwRTI130_assertion SIO_000772 8575754 NP1346353.RAKv72fJotrhNMbDFjXKPVFpE16f39z-ZFwVld_unwRTI130_provenance.
- NP1346353.RAKv72fJotrhNMbDFjXKPVFpE16f39z-ZFwVld_unwRTI130_assertion wasDerivedFrom befree-2016 NP1346353.RAKv72fJotrhNMbDFjXKPVFpE16f39z-ZFwVld_unwRTI130_provenance.
- NP1346353.RAKv72fJotrhNMbDFjXKPVFpE16f39z-ZFwVld_unwRTI130_assertion wasGeneratedBy ECO_0000203 NP1346353.RAKv72fJotrhNMbDFjXKPVFpE16f39z-ZFwVld_unwRTI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1346353.RAKv72fJotrhNMbDFjXKPVFpE16f39z-ZFwVld_unwRTI130_provenance.