Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_provenance.
- NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_assertion description "[Steroid 21-hydroxylase deficiency is the most common enzymatic defect causing congenital adrenal hyperplasia with genotype/phenotype relationships for common mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_provenance.
- NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_assertion evidence source_evidence_literature NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_provenance.
- NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_assertion SIO_000772 20080860 NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_provenance.
- NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_assertion wasDerivedFrom befree-2016 NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_provenance.
- NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_assertion wasGeneratedBy ECO_0000203 NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_provenance.
- befree-2016 importedOn "2016-02-19" NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_provenance.