Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_provenance.
- NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_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." NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_provenance.
- NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_assertion evidence source_evidence_literature NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_provenance.
- NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_assertion SIO_000772 21340157 NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_provenance.
- NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_assertion wasDerivedFrom befree-20150227 NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_provenance.
- NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_assertion wasGeneratedBy ECO_0000203 NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_provenance.
- befree-20150227 importedOn "2015-02-27" NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_provenance.