Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP156573.RAP4DbF6QbI3SGGIhIGjIQfI2ryAzH6Y8rqUAXFLAuT_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP156573.RAP4DbF6QbI3SGGIhIGjIQfI2ryAzH6Y8rqUAXFLAuT_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP156573.RAP4DbF6QbI3SGGIhIGjIQfI2ryAzH6Y8rqUAXFLAuT_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP156573.RAP4DbF6QbI3SGGIhIGjIQfI2ryAzH6Y8rqUAXFLAuT_s130_provenance.
- NP156573.RAP4DbF6QbI3SGGIhIGjIQfI2ryAzH6Y8rqUAXFLAuT_s130_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." NP156573.RAP4DbF6QbI3SGGIhIGjIQfI2ryAzH6Y8rqUAXFLAuT_s130_provenance.
- NP156573.RAP4DbF6QbI3SGGIhIGjIQfI2ryAzH6Y8rqUAXFLAuT_s130_assertion evidence source_evidence_literature NP156573.RAP4DbF6QbI3SGGIhIGjIQfI2ryAzH6Y8rqUAXFLAuT_s130_provenance.
- NP156573.RAP4DbF6QbI3SGGIhIGjIQfI2ryAzH6Y8rqUAXFLAuT_s130_assertion SIO_000772 16266991 NP156573.RAP4DbF6QbI3SGGIhIGjIQfI2ryAzH6Y8rqUAXFLAuT_s130_provenance.
- NP156573.RAP4DbF6QbI3SGGIhIGjIQfI2ryAzH6Y8rqUAXFLAuT_s130_assertion wasDerivedFrom befree-20140225 NP156573.RAP4DbF6QbI3SGGIhIGjIQfI2ryAzH6Y8rqUAXFLAuT_s130_provenance.
- NP156573.RAP4DbF6QbI3SGGIhIGjIQfI2ryAzH6Y8rqUAXFLAuT_s130_assertion wasGeneratedBy ECO_0000203 NP156573.RAP4DbF6QbI3SGGIhIGjIQfI2ryAzH6Y8rqUAXFLAuT_s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP156573.RAP4DbF6QbI3SGGIhIGjIQfI2ryAzH6Y8rqUAXFLAuT_s130_provenance.