Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6453.RAcBhvs6Ep25i1M4819apDbCY4O7wOVk1cQDUQMBM6bzw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6453.RAcBhvs6Ep25i1M4819apDbCY4O7wOVk1cQDUQMBM6bzw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6453.RAcBhvs6Ep25i1M4819apDbCY4O7wOVk1cQDUQMBM6bzw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6453.RAcBhvs6Ep25i1M4819apDbCY4O7wOVk1cQDUQMBM6bzw130_provenance.
- NP6453.RAcBhvs6Ep25i1M4819apDbCY4O7wOVk1cQDUQMBM6bzw130_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." NP6453.RAcBhvs6Ep25i1M4819apDbCY4O7wOVk1cQDUQMBM6bzw130_provenance.
- NP6453.RAcBhvs6Ep25i1M4819apDbCY4O7wOVk1cQDUQMBM6bzw130_assertion evidence source_evidence_curated NP6453.RAcBhvs6Ep25i1M4819apDbCY4O7wOVk1cQDUQMBM6bzw130_provenance.
- NP6453.RAcBhvs6Ep25i1M4819apDbCY4O7wOVk1cQDUQMBM6bzw130_assertion SIO_000772 21129722 NP6453.RAcBhvs6Ep25i1M4819apDbCY4O7wOVk1cQDUQMBM6bzw130_provenance.
- NP6453.RAcBhvs6Ep25i1M4819apDbCY4O7wOVk1cQDUQMBM6bzw130_assertion wasDerivedFrom uniprot-2016 NP6453.RAcBhvs6Ep25i1M4819apDbCY4O7wOVk1cQDUQMBM6bzw130_provenance.
- NP6453.RAcBhvs6Ep25i1M4819apDbCY4O7wOVk1cQDUQMBM6bzw130_assertion wasGeneratedBy ECO_0000218 NP6453.RAcBhvs6Ep25i1M4819apDbCY4O7wOVk1cQDUQMBM6bzw130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6453.RAcBhvs6Ep25i1M4819apDbCY4O7wOVk1cQDUQMBM6bzw130_provenance.