Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_provenance.
- NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_assertion wasGeneratedBy ECO_0000203 NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_provenance.
- NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_assertion wasDerivedFrom befree-20140225 NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_provenance.
- NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_assertion SIO_000772 9305598 NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_provenance.
- NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_assertion evidence source_evidence_literature NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_provenance.
- NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_assertion description "[In this series of unselected patients, LOH of ETV6 markers was found in 23% of cases (6% of T-ALL and 26% of B lineage ALL) confirming that chromosome 12p12-13 deletions represent a major genetic alteration in childhood ALL, frequently missed by cytogenetic analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_provenance.