Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP377471.RAL6U7OSq6LZNc4PcWBJD48niCip96HzmRtaDM-aOft2M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP377471.RAL6U7OSq6LZNc4PcWBJD48niCip96HzmRtaDM-aOft2M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP377471.RAL6U7OSq6LZNc4PcWBJD48niCip96HzmRtaDM-aOft2M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP377471.RAL6U7OSq6LZNc4PcWBJD48niCip96HzmRtaDM-aOft2M130_provenance.
- NP377471.RAL6U7OSq6LZNc4PcWBJD48niCip96HzmRtaDM-aOft2M130_assertion description "[To better understand the mechanisms of P450c17 deficiency, we studied 2 patients (both 46,XY) with combined 17alpha-hydroxylase/17,20-lyase deficiency of different severity: one with complete lack of masculinization and one with ambiguous genitalia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP377471.RAL6U7OSq6LZNc4PcWBJD48niCip96HzmRtaDM-aOft2M130_provenance.
- NP377471.RAL6U7OSq6LZNc4PcWBJD48niCip96HzmRtaDM-aOft2M130_assertion evidence source_evidence_literature NP377471.RAL6U7OSq6LZNc4PcWBJD48niCip96HzmRtaDM-aOft2M130_provenance.
- NP377471.RAL6U7OSq6LZNc4PcWBJD48niCip96HzmRtaDM-aOft2M130_assertion SIO_000772 20197673 NP377471.RAL6U7OSq6LZNc4PcWBJD48niCip96HzmRtaDM-aOft2M130_provenance.
- NP377471.RAL6U7OSq6LZNc4PcWBJD48niCip96HzmRtaDM-aOft2M130_assertion wasDerivedFrom befree-20140225 NP377471.RAL6U7OSq6LZNc4PcWBJD48niCip96HzmRtaDM-aOft2M130_provenance.
- NP377471.RAL6U7OSq6LZNc4PcWBJD48niCip96HzmRtaDM-aOft2M130_assertion wasGeneratedBy ECO_0000203 NP377471.RAL6U7OSq6LZNc4PcWBJD48niCip96HzmRtaDM-aOft2M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP377471.RAL6U7OSq6LZNc4PcWBJD48niCip96HzmRtaDM-aOft2M130_provenance.