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- source_evidence_literature type ECO_0000212 NP969421.RAtKfLzyYVABcfuj5-nIF6nlvc-2z_sr4GlG5X0UPlPzk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP969421.RAtKfLzyYVABcfuj5-nIF6nlvc-2z_sr4GlG5X0UPlPzk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP969421.RAtKfLzyYVABcfuj5-nIF6nlvc-2z_sr4GlG5X0UPlPzk130_provenance.
- NP969421.RAtKfLzyYVABcfuj5-nIF6nlvc-2z_sr4GlG5X0UPlPzk130_assertion description "[In initial and validation analyses, SLX4IP deletions were significantly associated with male gender and ETV6/RUNX1-rearranged ALL (both overall P < 0.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP969421.RAtKfLzyYVABcfuj5-nIF6nlvc-2z_sr4GlG5X0UPlPzk130_provenance.
- NP969421.RAtKfLzyYVABcfuj5-nIF6nlvc-2z_sr4GlG5X0UPlPzk130_assertion evidence source_evidence_literature NP969421.RAtKfLzyYVABcfuj5-nIF6nlvc-2z_sr4GlG5X0UPlPzk130_provenance.
- NP969421.RAtKfLzyYVABcfuj5-nIF6nlvc-2z_sr4GlG5X0UPlPzk130_assertion SIO_000772 24045615 NP969421.RAtKfLzyYVABcfuj5-nIF6nlvc-2z_sr4GlG5X0UPlPzk130_provenance.
- NP969421.RAtKfLzyYVABcfuj5-nIF6nlvc-2z_sr4GlG5X0UPlPzk130_assertion wasDerivedFrom befree-20150227 NP969421.RAtKfLzyYVABcfuj5-nIF6nlvc-2z_sr4GlG5X0UPlPzk130_provenance.
- NP969421.RAtKfLzyYVABcfuj5-nIF6nlvc-2z_sr4GlG5X0UPlPzk130_assertion wasGeneratedBy ECO_0000203 NP969421.RAtKfLzyYVABcfuj5-nIF6nlvc-2z_sr4GlG5X0UPlPzk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP969421.RAtKfLzyYVABcfuj5-nIF6nlvc-2z_sr4GlG5X0UPlPzk130_provenance.