Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_provenance.
- NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_assertion description "[reported 24 patients from 19 Brazilian families with 17?-hydroxylase deficiency and showed that p.W406R and p.R362C corresponded to 50% and 32% of CYP17A1 mutant alleles, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_provenance.
- NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_assertion evidence source_evidence_literature NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_provenance.
- NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_assertion SIO_000772 21340157 NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_provenance.
- NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_assertion wasDerivedFrom befree-20140225 NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_provenance.
- NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_assertion wasGeneratedBy ECO_0000203 NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_provenance.