Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP3914.RA5xVDRtht0vQf9iI6oxRG1TjM-hV-G3hRPFJDLeR_rMM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3914.RA5xVDRtht0vQf9iI6oxRG1TjM-hV-G3hRPFJDLeR_rMM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3914.RA5xVDRtht0vQf9iI6oxRG1TjM-hV-G3hRPFJDLeR_rMM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3914.RA5xVDRtht0vQf9iI6oxRG1TjM-hV-G3hRPFJDLeR_rMM130_provenance.
- NP3914.RA5xVDRtht0vQf9iI6oxRG1TjM-hV-G3hRPFJDLeR_rMM130_assertion description "[Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3914.RA5xVDRtht0vQf9iI6oxRG1TjM-hV-G3hRPFJDLeR_rMM130_provenance.
- NP3914.RA5xVDRtht0vQf9iI6oxRG1TjM-hV-G3hRPFJDLeR_rMM130_assertion evidence source_evidence_curated NP3914.RA5xVDRtht0vQf9iI6oxRG1TjM-hV-G3hRPFJDLeR_rMM130_provenance.
- NP3914.RA5xVDRtht0vQf9iI6oxRG1TjM-hV-G3hRPFJDLeR_rMM130_assertion SIO_000772 21129722 NP3914.RA5xVDRtht0vQf9iI6oxRG1TjM-hV-G3hRPFJDLeR_rMM130_provenance.
- NP3914.RA5xVDRtht0vQf9iI6oxRG1TjM-hV-G3hRPFJDLeR_rMM130_assertion wasDerivedFrom uniprot-20130724 NP3914.RA5xVDRtht0vQf9iI6oxRG1TjM-hV-G3hRPFJDLeR_rMM130_provenance.
- NP3914.RA5xVDRtht0vQf9iI6oxRG1TjM-hV-G3hRPFJDLeR_rMM130_assertion wasGeneratedBy ECO_0000218 NP3914.RA5xVDRtht0vQf9iI6oxRG1TjM-hV-G3hRPFJDLeR_rMM130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP3914.RA5xVDRtht0vQf9iI6oxRG1TjM-hV-G3hRPFJDLeR_rMM130_provenance.