Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP156635.RA-sXw7tbStggW4xnO4GysfV4udi80RA4QOjMi-GtAprI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP156635.RA-sXw7tbStggW4xnO4GysfV4udi80RA4QOjMi-GtAprI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP156635.RA-sXw7tbStggW4xnO4GysfV4udi80RA4QOjMi-GtAprI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP156635.RA-sXw7tbStggW4xnO4GysfV4udi80RA4QOjMi-GtAprI130_provenance.
- NP156635.RA-sXw7tbStggW4xnO4GysfV4udi80RA4QOjMi-GtAprI130_assertion description "[Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11beta-hydroxylase) and CYP11B2(aldosterone synthase) cause steroid 11beta-hydroxylase deficiency and congenital adrenal hyperplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156635.RA-sXw7tbStggW4xnO4GysfV4udi80RA4QOjMi-GtAprI130_provenance.
- NP156635.RA-sXw7tbStggW4xnO4GysfV4udi80RA4QOjMi-GtAprI130_assertion evidence source_evidence_literature NP156635.RA-sXw7tbStggW4xnO4GysfV4udi80RA4QOjMi-GtAprI130_provenance.
- NP156635.RA-sXw7tbStggW4xnO4GysfV4udi80RA4QOjMi-GtAprI130_assertion SIO_000772 11443188 NP156635.RA-sXw7tbStggW4xnO4GysfV4udi80RA4QOjMi-GtAprI130_provenance.
- NP156635.RA-sXw7tbStggW4xnO4GysfV4udi80RA4QOjMi-GtAprI130_assertion wasDerivedFrom befree-20140225 NP156635.RA-sXw7tbStggW4xnO4GysfV4udi80RA4QOjMi-GtAprI130_provenance.
- NP156635.RA-sXw7tbStggW4xnO4GysfV4udi80RA4QOjMi-GtAprI130_assertion wasGeneratedBy ECO_0000203 NP156635.RA-sXw7tbStggW4xnO4GysfV4udi80RA4QOjMi-GtAprI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP156635.RA-sXw7tbStggW4xnO4GysfV4udi80RA4QOjMi-GtAprI130_provenance.