Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP435413.RAJ8XzUZylHxnwLAWFtD2M0fw5_1WTCf_9T2INIXYXx0E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP435413.RAJ8XzUZylHxnwLAWFtD2M0fw5_1WTCf_9T2INIXYXx0E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435413.RAJ8XzUZylHxnwLAWFtD2M0fw5_1WTCf_9T2INIXYXx0E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435413.RAJ8XzUZylHxnwLAWFtD2M0fw5_1WTCf_9T2INIXYXx0E130_provenance.
- NP435413.RAJ8XzUZylHxnwLAWFtD2M0fw5_1WTCf_9T2INIXYXx0E130_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." NP435413.RAJ8XzUZylHxnwLAWFtD2M0fw5_1WTCf_9T2INIXYXx0E130_provenance.
- NP435413.RAJ8XzUZylHxnwLAWFtD2M0fw5_1WTCf_9T2INIXYXx0E130_assertion evidence source_evidence_literature NP435413.RAJ8XzUZylHxnwLAWFtD2M0fw5_1WTCf_9T2INIXYXx0E130_provenance.
- NP435413.RAJ8XzUZylHxnwLAWFtD2M0fw5_1WTCf_9T2INIXYXx0E130_assertion SIO_000772 16266991 NP435413.RAJ8XzUZylHxnwLAWFtD2M0fw5_1WTCf_9T2INIXYXx0E130_provenance.
- NP435413.RAJ8XzUZylHxnwLAWFtD2M0fw5_1WTCf_9T2INIXYXx0E130_assertion wasDerivedFrom befree-20150227 NP435413.RAJ8XzUZylHxnwLAWFtD2M0fw5_1WTCf_9T2INIXYXx0E130_provenance.
- NP435413.RAJ8XzUZylHxnwLAWFtD2M0fw5_1WTCf_9T2INIXYXx0E130_assertion wasGeneratedBy ECO_0000203 NP435413.RAJ8XzUZylHxnwLAWFtD2M0fw5_1WTCf_9T2INIXYXx0E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP435413.RAJ8XzUZylHxnwLAWFtD2M0fw5_1WTCf_9T2INIXYXx0E130_provenance.