Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246122.RAW0hHCSL5BviPGplvLb7PKb6TD6HnWYujh9UJmwlLmh4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1246122.RAW0hHCSL5BviPGplvLb7PKb6TD6HnWYujh9UJmwlLmh4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246122.RAW0hHCSL5BviPGplvLb7PKb6TD6HnWYujh9UJmwlLmh4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246122.RAW0hHCSL5BviPGplvLb7PKb6TD6HnWYujh9UJmwlLmh4130_provenance.
- NP1246122.RAW0hHCSL5BviPGplvLb7PKb6TD6HnWYujh9UJmwlLmh4130_assertion description "[No IDH1 R132 and IDH2 R172 mutations were identified in the entire cohort, whereas IDH1 G105G allele was detected in 4/108 MPN (3.70%), 2/22 MDS (9.09%), and 2/41 PNH (4.88%) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246122.RAW0hHCSL5BviPGplvLb7PKb6TD6HnWYujh9UJmwlLmh4130_provenance.
- NP1246122.RAW0hHCSL5BviPGplvLb7PKb6TD6HnWYujh9UJmwlLmh4130_assertion evidence source_evidence_literature NP1246122.RAW0hHCSL5BviPGplvLb7PKb6TD6HnWYujh9UJmwlLmh4130_provenance.
- NP1246122.RAW0hHCSL5BviPGplvLb7PKb6TD6HnWYujh9UJmwlLmh4130_assertion SIO_000772 25486927 NP1246122.RAW0hHCSL5BviPGplvLb7PKb6TD6HnWYujh9UJmwlLmh4130_provenance.
- NP1246122.RAW0hHCSL5BviPGplvLb7PKb6TD6HnWYujh9UJmwlLmh4130_assertion wasDerivedFrom befree-2016 NP1246122.RAW0hHCSL5BviPGplvLb7PKb6TD6HnWYujh9UJmwlLmh4130_provenance.
- NP1246122.RAW0hHCSL5BviPGplvLb7PKb6TD6HnWYujh9UJmwlLmh4130_assertion wasGeneratedBy ECO_0000203 NP1246122.RAW0hHCSL5BviPGplvLb7PKb6TD6HnWYujh9UJmwlLmh4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246122.RAW0hHCSL5BviPGplvLb7PKb6TD6HnWYujh9UJmwlLmh4130_provenance.