Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP552819.RAOqBKlllC6m6Ggxx1fWrMveSzEh4w7a6lqst9zNHVkUE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP552819.RAOqBKlllC6m6Ggxx1fWrMveSzEh4w7a6lqst9zNHVkUE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP552819.RAOqBKlllC6m6Ggxx1fWrMveSzEh4w7a6lqst9zNHVkUE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP552819.RAOqBKlllC6m6Ggxx1fWrMveSzEh4w7a6lqst9zNHVkUE130_provenance.
- NP552819.RAOqBKlllC6m6Ggxx1fWrMveSzEh4w7a6lqst9zNHVkUE130_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." NP552819.RAOqBKlllC6m6Ggxx1fWrMveSzEh4w7a6lqst9zNHVkUE130_provenance.
- NP552819.RAOqBKlllC6m6Ggxx1fWrMveSzEh4w7a6lqst9zNHVkUE130_assertion evidence source_evidence_literature NP552819.RAOqBKlllC6m6Ggxx1fWrMveSzEh4w7a6lqst9zNHVkUE130_provenance.
- NP552819.RAOqBKlllC6m6Ggxx1fWrMveSzEh4w7a6lqst9zNHVkUE130_assertion SIO_000772 21129722 NP552819.RAOqBKlllC6m6Ggxx1fWrMveSzEh4w7a6lqst9zNHVkUE130_provenance.
- NP552819.RAOqBKlllC6m6Ggxx1fWrMveSzEh4w7a6lqst9zNHVkUE130_assertion wasDerivedFrom befree-20150227 NP552819.RAOqBKlllC6m6Ggxx1fWrMveSzEh4w7a6lqst9zNHVkUE130_provenance.
- NP552819.RAOqBKlllC6m6Ggxx1fWrMveSzEh4w7a6lqst9zNHVkUE130_assertion wasGeneratedBy ECO_0000203 NP552819.RAOqBKlllC6m6Ggxx1fWrMveSzEh4w7a6lqst9zNHVkUE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP552819.RAOqBKlllC6m6Ggxx1fWrMveSzEh4w7a6lqst9zNHVkUE130_provenance.