Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP856837.RAbbcVuMlnDwb9OrtsAYHqQyjWZvgUgt0m2uToXBOfCqA130_assertion> ?p ?o ?g. }
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- NP856837.RAbbcVuMlnDwb9OrtsAYHqQyjWZvgUgt0m2uToXBOfCqA130_assertion type Assertion NP856837.RAbbcVuMlnDwb9OrtsAYHqQyjWZvgUgt0m2uToXBOfCqA130_head.
- NP856837.RAbbcVuMlnDwb9OrtsAYHqQyjWZvgUgt0m2uToXBOfCqA130_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." NP856837.RAbbcVuMlnDwb9OrtsAYHqQyjWZvgUgt0m2uToXBOfCqA130_provenance.
- NP856837.RAbbcVuMlnDwb9OrtsAYHqQyjWZvgUgt0m2uToXBOfCqA130_assertion evidence source_evidence_literature NP856837.RAbbcVuMlnDwb9OrtsAYHqQyjWZvgUgt0m2uToXBOfCqA130_provenance.
- NP856837.RAbbcVuMlnDwb9OrtsAYHqQyjWZvgUgt0m2uToXBOfCqA130_assertion SIO_000772 21129722 NP856837.RAbbcVuMlnDwb9OrtsAYHqQyjWZvgUgt0m2uToXBOfCqA130_provenance.
- NP856837.RAbbcVuMlnDwb9OrtsAYHqQyjWZvgUgt0m2uToXBOfCqA130_assertion wasDerivedFrom befree-2016 NP856837.RAbbcVuMlnDwb9OrtsAYHqQyjWZvgUgt0m2uToXBOfCqA130_provenance.
- NP856837.RAbbcVuMlnDwb9OrtsAYHqQyjWZvgUgt0m2uToXBOfCqA130_assertion wasGeneratedBy ECO_0000203 NP856837.RAbbcVuMlnDwb9OrtsAYHqQyjWZvgUgt0m2uToXBOfCqA130_provenance.