Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP752616.RAB_qsl8Ui0RjQTeGUjucAoan_Oki5e4Nmk-joln4YYwQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP752616.RAB_qsl8Ui0RjQTeGUjucAoan_Oki5e4Nmk-joln4YYwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP752616.RAB_qsl8Ui0RjQTeGUjucAoan_Oki5e4Nmk-joln4YYwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP752616.RAB_qsl8Ui0RjQTeGUjucAoan_Oki5e4Nmk-joln4YYwQ130_provenance.
- NP752616.RAB_qsl8Ui0RjQTeGUjucAoan_Oki5e4Nmk-joln4YYwQ130_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." NP752616.RAB_qsl8Ui0RjQTeGUjucAoan_Oki5e4Nmk-joln4YYwQ130_provenance.
- NP752616.RAB_qsl8Ui0RjQTeGUjucAoan_Oki5e4Nmk-joln4YYwQ130_assertion evidence source_evidence_literature NP752616.RAB_qsl8Ui0RjQTeGUjucAoan_Oki5e4Nmk-joln4YYwQ130_provenance.
- NP752616.RAB_qsl8Ui0RjQTeGUjucAoan_Oki5e4Nmk-joln4YYwQ130_assertion SIO_000772 21129722 NP752616.RAB_qsl8Ui0RjQTeGUjucAoan_Oki5e4Nmk-joln4YYwQ130_provenance.
- NP752616.RAB_qsl8Ui0RjQTeGUjucAoan_Oki5e4Nmk-joln4YYwQ130_assertion wasDerivedFrom befree-20140225 NP752616.RAB_qsl8Ui0RjQTeGUjucAoan_Oki5e4Nmk-joln4YYwQ130_provenance.
- NP752616.RAB_qsl8Ui0RjQTeGUjucAoan_Oki5e4Nmk-joln4YYwQ130_assertion wasGeneratedBy ECO_0000203 NP752616.RAB_qsl8Ui0RjQTeGUjucAoan_Oki5e4Nmk-joln4YYwQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP752616.RAB_qsl8Ui0RjQTeGUjucAoan_Oki5e4Nmk-joln4YYwQ130_provenance.