Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP856832.RAk8yd7Xpv9PXXyFmS31n0cpF0SEQZtaH8W_TEQjr-T6w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP856832.RAk8yd7Xpv9PXXyFmS31n0cpF0SEQZtaH8W_TEQjr-T6w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP856832.RAk8yd7Xpv9PXXyFmS31n0cpF0SEQZtaH8W_TEQjr-T6w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP856832.RAk8yd7Xpv9PXXyFmS31n0cpF0SEQZtaH8W_TEQjr-T6w130_provenance.
- NP856832.RAk8yd7Xpv9PXXyFmS31n0cpF0SEQZtaH8W_TEQjr-T6w130_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." NP856832.RAk8yd7Xpv9PXXyFmS31n0cpF0SEQZtaH8W_TEQjr-T6w130_provenance.
- NP856832.RAk8yd7Xpv9PXXyFmS31n0cpF0SEQZtaH8W_TEQjr-T6w130_assertion evidence source_evidence_literature NP856832.RAk8yd7Xpv9PXXyFmS31n0cpF0SEQZtaH8W_TEQjr-T6w130_provenance.
- NP856832.RAk8yd7Xpv9PXXyFmS31n0cpF0SEQZtaH8W_TEQjr-T6w130_assertion SIO_000772 21129722 NP856832.RAk8yd7Xpv9PXXyFmS31n0cpF0SEQZtaH8W_TEQjr-T6w130_provenance.
- NP856832.RAk8yd7Xpv9PXXyFmS31n0cpF0SEQZtaH8W_TEQjr-T6w130_assertion wasDerivedFrom befree-2016 NP856832.RAk8yd7Xpv9PXXyFmS31n0cpF0SEQZtaH8W_TEQjr-T6w130_provenance.
- NP856832.RAk8yd7Xpv9PXXyFmS31n0cpF0SEQZtaH8W_TEQjr-T6w130_assertion wasGeneratedBy ECO_0000203 NP856832.RAk8yd7Xpv9PXXyFmS31n0cpF0SEQZtaH8W_TEQjr-T6w130_provenance.
- befree-2016 importedOn "2016-02-19" NP856832.RAk8yd7Xpv9PXXyFmS31n0cpF0SEQZtaH8W_TEQjr-T6w130_provenance.