Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP520816.RA5Ud27WcjVGt-NWocL-lef5y_RNpuX-uGYQPEknEAZzI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP520816.RA5Ud27WcjVGt-NWocL-lef5y_RNpuX-uGYQPEknEAZzI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP520816.RA5Ud27WcjVGt-NWocL-lef5y_RNpuX-uGYQPEknEAZzI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP520816.RA5Ud27WcjVGt-NWocL-lef5y_RNpuX-uGYQPEknEAZzI130_provenance.
- NP520816.RA5Ud27WcjVGt-NWocL-lef5y_RNpuX-uGYQPEknEAZzI130_assertion description "[However, we report the second case of ALL with a somatic mutation of the GR involving a 29-bp deletion in exon 8 and resulting in a truncated protein with loss of part of the ligand-binding domain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP520816.RA5Ud27WcjVGt-NWocL-lef5y_RNpuX-uGYQPEknEAZzI130_provenance.
- NP520816.RA5Ud27WcjVGt-NWocL-lef5y_RNpuX-uGYQPEknEAZzI130_assertion evidence source_evidence_literature NP520816.RA5Ud27WcjVGt-NWocL-lef5y_RNpuX-uGYQPEknEAZzI130_provenance.
- NP520816.RA5Ud27WcjVGt-NWocL-lef5y_RNpuX-uGYQPEknEAZzI130_assertion SIO_000772 16266991 NP520816.RA5Ud27WcjVGt-NWocL-lef5y_RNpuX-uGYQPEknEAZzI130_provenance.
- NP520816.RA5Ud27WcjVGt-NWocL-lef5y_RNpuX-uGYQPEknEAZzI130_assertion wasDerivedFrom befree-2016 NP520816.RA5Ud27WcjVGt-NWocL-lef5y_RNpuX-uGYQPEknEAZzI130_provenance.
- NP520816.RA5Ud27WcjVGt-NWocL-lef5y_RNpuX-uGYQPEknEAZzI130_assertion wasGeneratedBy ECO_0000203 NP520816.RA5Ud27WcjVGt-NWocL-lef5y_RNpuX-uGYQPEknEAZzI130_provenance.
- befree-2016 importedOn "2016-02-19" NP520816.RA5Ud27WcjVGt-NWocL-lef5y_RNpuX-uGYQPEknEAZzI130_provenance.