Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP754058.RAH9pmTL6bdOKseA6HnEqAe_nvznCKqCMzXPmoALJhxmc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP754058.RAH9pmTL6bdOKseA6HnEqAe_nvznCKqCMzXPmoALJhxmc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP754058.RAH9pmTL6bdOKseA6HnEqAe_nvznCKqCMzXPmoALJhxmc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP754058.RAH9pmTL6bdOKseA6HnEqAe_nvznCKqCMzXPmoALJhxmc130_provenance.
- NP754058.RAH9pmTL6bdOKseA6HnEqAe_nvznCKqCMzXPmoALJhxmc130_assertion description "[Cap43 promoter assays with several deletion or mutation constructs demonstrated that the Sp1 site in the element from -286 base pairs (bp) to -62 bp was partly responsible for VHL-induced suppression of the Cap43 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP754058.RAH9pmTL6bdOKseA6HnEqAe_nvznCKqCMzXPmoALJhxmc130_provenance.
- NP754058.RAH9pmTL6bdOKseA6HnEqAe_nvznCKqCMzXPmoALJhxmc130_assertion evidence source_evidence_literature NP754058.RAH9pmTL6bdOKseA6HnEqAe_nvznCKqCMzXPmoALJhxmc130_provenance.
- NP754058.RAH9pmTL6bdOKseA6HnEqAe_nvznCKqCMzXPmoALJhxmc130_assertion SIO_000772 12767066 NP754058.RAH9pmTL6bdOKseA6HnEqAe_nvznCKqCMzXPmoALJhxmc130_provenance.
- NP754058.RAH9pmTL6bdOKseA6HnEqAe_nvznCKqCMzXPmoALJhxmc130_assertion wasDerivedFrom befree-20140225 NP754058.RAH9pmTL6bdOKseA6HnEqAe_nvznCKqCMzXPmoALJhxmc130_provenance.
- NP754058.RAH9pmTL6bdOKseA6HnEqAe_nvznCKqCMzXPmoALJhxmc130_assertion wasGeneratedBy ECO_0000203 NP754058.RAH9pmTL6bdOKseA6HnEqAe_nvznCKqCMzXPmoALJhxmc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP754058.RAH9pmTL6bdOKseA6HnEqAe_nvznCKqCMzXPmoALJhxmc130_provenance.