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- source_evidence_literature type ECO_0000212 NP552827.RAnxXXKv9z0UKAN1e1i51D1fZS0mt2_Za1LlyvZlQmfyo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP552827.RAnxXXKv9z0UKAN1e1i51D1fZS0mt2_Za1LlyvZlQmfyo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP552827.RAnxXXKv9z0UKAN1e1i51D1fZS0mt2_Za1LlyvZlQmfyo130_provenance.
- NP552827.RAnxXXKv9z0UKAN1e1i51D1fZS0mt2_Za1LlyvZlQmfyo130_assertion description "[Thus, mutations in MAP3K1 that result in 46,XY DSD with partial or complete gonadal dysgenesis implicate this pathway in normal human sex determination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552827.RAnxXXKv9z0UKAN1e1i51D1fZS0mt2_Za1LlyvZlQmfyo130_provenance.
- NP552827.RAnxXXKv9z0UKAN1e1i51D1fZS0mt2_Za1LlyvZlQmfyo130_assertion evidence source_evidence_literature NP552827.RAnxXXKv9z0UKAN1e1i51D1fZS0mt2_Za1LlyvZlQmfyo130_provenance.
- NP552827.RAnxXXKv9z0UKAN1e1i51D1fZS0mt2_Za1LlyvZlQmfyo130_assertion SIO_000772 21129722 NP552827.RAnxXXKv9z0UKAN1e1i51D1fZS0mt2_Za1LlyvZlQmfyo130_provenance.
- NP552827.RAnxXXKv9z0UKAN1e1i51D1fZS0mt2_Za1LlyvZlQmfyo130_assertion wasDerivedFrom befree-20150227 NP552827.RAnxXXKv9z0UKAN1e1i51D1fZS0mt2_Za1LlyvZlQmfyo130_provenance.
- NP552827.RAnxXXKv9z0UKAN1e1i51D1fZS0mt2_Za1LlyvZlQmfyo130_assertion wasGeneratedBy ECO_0000203 NP552827.RAnxXXKv9z0UKAN1e1i51D1fZS0mt2_Za1LlyvZlQmfyo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP552827.RAnxXXKv9z0UKAN1e1i51D1fZS0mt2_Za1LlyvZlQmfyo130_provenance.