Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP520815.RAL7D55NeQk64txH4oYSGTeyF5e30Cd5wrIIRxDUJavs8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP520815.RAL7D55NeQk64txH4oYSGTeyF5e30Cd5wrIIRxDUJavs8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP520815.RAL7D55NeQk64txH4oYSGTeyF5e30Cd5wrIIRxDUJavs8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP520815.RAL7D55NeQk64txH4oYSGTeyF5e30Cd5wrIIRxDUJavs8130_provenance.
- NP520815.RAL7D55NeQk64txH4oYSGTeyF5e30Cd5wrIIRxDUJavs8130_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." NP520815.RAL7D55NeQk64txH4oYSGTeyF5e30Cd5wrIIRxDUJavs8130_provenance.
- NP520815.RAL7D55NeQk64txH4oYSGTeyF5e30Cd5wrIIRxDUJavs8130_assertion evidence source_evidence_literature NP520815.RAL7D55NeQk64txH4oYSGTeyF5e30Cd5wrIIRxDUJavs8130_provenance.
- NP520815.RAL7D55NeQk64txH4oYSGTeyF5e30Cd5wrIIRxDUJavs8130_assertion SIO_000772 16266991 NP520815.RAL7D55NeQk64txH4oYSGTeyF5e30Cd5wrIIRxDUJavs8130_provenance.
- NP520815.RAL7D55NeQk64txH4oYSGTeyF5e30Cd5wrIIRxDUJavs8130_assertion wasDerivedFrom befree-2016 NP520815.RAL7D55NeQk64txH4oYSGTeyF5e30Cd5wrIIRxDUJavs8130_provenance.
- NP520815.RAL7D55NeQk64txH4oYSGTeyF5e30Cd5wrIIRxDUJavs8130_assertion wasGeneratedBy ECO_0000203 NP520815.RAL7D55NeQk64txH4oYSGTeyF5e30Cd5wrIIRxDUJavs8130_provenance.
- befree-2016 importedOn "2016-02-19" NP520815.RAL7D55NeQk64txH4oYSGTeyF5e30Cd5wrIIRxDUJavs8130_provenance.