Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP413535.RAgcgGLz1BP1iHBDVYCCBBpvv6moCj1mSrp5B5Y2PPjvg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP413535.RAgcgGLz1BP1iHBDVYCCBBpvv6moCj1mSrp5B5Y2PPjvg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP413535.RAgcgGLz1BP1iHBDVYCCBBpvv6moCj1mSrp5B5Y2PPjvg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP413535.RAgcgGLz1BP1iHBDVYCCBBpvv6moCj1mSrp5B5Y2PPjvg130_provenance.
- NP413535.RAgcgGLz1BP1iHBDVYCCBBpvv6moCj1mSrp5B5Y2PPjvg130_assertion description "[A group of 100 46,XY DSD and two POI was studied for NR5A1 mutations and their impact.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP413535.RAgcgGLz1BP1iHBDVYCCBBpvv6moCj1mSrp5B5Y2PPjvg130_provenance.
- NP413535.RAgcgGLz1BP1iHBDVYCCBBpvv6moCj1mSrp5B5Y2PPjvg130_assertion evidence source_evidence_literature NP413535.RAgcgGLz1BP1iHBDVYCCBBpvv6moCj1mSrp5B5Y2PPjvg130_provenance.
- NP413535.RAgcgGLz1BP1iHBDVYCCBBpvv6moCj1mSrp5B5Y2PPjvg130_assertion SIO_000772 22549935 NP413535.RAgcgGLz1BP1iHBDVYCCBBpvv6moCj1mSrp5B5Y2PPjvg130_provenance.
- NP413535.RAgcgGLz1BP1iHBDVYCCBBpvv6moCj1mSrp5B5Y2PPjvg130_assertion wasDerivedFrom befree-20150227 NP413535.RAgcgGLz1BP1iHBDVYCCBBpvv6moCj1mSrp5B5Y2PPjvg130_provenance.
- NP413535.RAgcgGLz1BP1iHBDVYCCBBpvv6moCj1mSrp5B5Y2PPjvg130_assertion wasGeneratedBy ECO_0000203 NP413535.RAgcgGLz1BP1iHBDVYCCBBpvv6moCj1mSrp5B5Y2PPjvg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP413535.RAgcgGLz1BP1iHBDVYCCBBpvv6moCj1mSrp5B5Y2PPjvg130_provenance.