Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_provenance.
- NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_assertion description "[To investigate the presence of mutations in the open reading frame (ORF), as well as on the 5' and 3', flanking regions of the SRY gene in patients with mixed gonadal dysgenesis (MGD) or with Turner syndrome (TS) and Y mosaicism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_provenance.
- NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_assertion evidence source_evidence_literature NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_provenance.
- NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_assertion SIO_000772 15223166 NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_provenance.
- NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_assertion wasDerivedFrom befree-20140225 NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_provenance.
- NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_assertion wasGeneratedBy ECO_0000203 NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_provenance.