Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP572794.RA0OOKmOLoNk-K1feGYsnjNv-FTfClm3VxJ-Lsy-I2FSY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP572794.RA0OOKmOLoNk-K1feGYsnjNv-FTfClm3VxJ-Lsy-I2FSY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP572794.RA0OOKmOLoNk-K1feGYsnjNv-FTfClm3VxJ-Lsy-I2FSY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP572794.RA0OOKmOLoNk-K1feGYsnjNv-FTfClm3VxJ-Lsy-I2FSY130_provenance.
- NP572794.RA0OOKmOLoNk-K1feGYsnjNv-FTfClm3VxJ-Lsy-I2FSY130_assertion description "[Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP572794.RA0OOKmOLoNk-K1feGYsnjNv-FTfClm3VxJ-Lsy-I2FSY130_provenance.
- NP572794.RA0OOKmOLoNk-K1feGYsnjNv-FTfClm3VxJ-Lsy-I2FSY130_assertion evidence source_evidence_literature NP572794.RA0OOKmOLoNk-K1feGYsnjNv-FTfClm3VxJ-Lsy-I2FSY130_provenance.
- NP572794.RA0OOKmOLoNk-K1feGYsnjNv-FTfClm3VxJ-Lsy-I2FSY130_assertion SIO_000772 21129722 NP572794.RA0OOKmOLoNk-K1feGYsnjNv-FTfClm3VxJ-Lsy-I2FSY130_provenance.
- NP572794.RA0OOKmOLoNk-K1feGYsnjNv-FTfClm3VxJ-Lsy-I2FSY130_assertion wasDerivedFrom befree-20140225 NP572794.RA0OOKmOLoNk-K1feGYsnjNv-FTfClm3VxJ-Lsy-I2FSY130_provenance.
- NP572794.RA0OOKmOLoNk-K1feGYsnjNv-FTfClm3VxJ-Lsy-I2FSY130_assertion wasGeneratedBy ECO_0000203 NP572794.RA0OOKmOLoNk-K1feGYsnjNv-FTfClm3VxJ-Lsy-I2FSY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP572794.RA0OOKmOLoNk-K1feGYsnjNv-FTfClm3VxJ-Lsy-I2FSY130_provenance.