Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP284605.RAQg1AKhu9GWFC1L6Fs2H91rLSv2BnL25dbk3ZLnTqkQ8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP284605.RAQg1AKhu9GWFC1L6Fs2H91rLSv2BnL25dbk3ZLnTqkQ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284605.RAQg1AKhu9GWFC1L6Fs2H91rLSv2BnL25dbk3ZLnTqkQ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284605.RAQg1AKhu9GWFC1L6Fs2H91rLSv2BnL25dbk3ZLnTqkQ8130_provenance.
- NP284605.RAQg1AKhu9GWFC1L6Fs2H91rLSv2BnL25dbk3ZLnTqkQ8130_assertion description "[Recurrence of a nonsense mutation in the conserved domain of SRY in a Brazilian patient with 46,XY gonadal dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284605.RAQg1AKhu9GWFC1L6Fs2H91rLSv2BnL25dbk3ZLnTqkQ8130_provenance.
- NP284605.RAQg1AKhu9GWFC1L6Fs2H91rLSv2BnL25dbk3ZLnTqkQ8130_assertion evidence source_evidence_literature NP284605.RAQg1AKhu9GWFC1L6Fs2H91rLSv2BnL25dbk3ZLnTqkQ8130_provenance.
- NP284605.RAQg1AKhu9GWFC1L6Fs2H91rLSv2BnL25dbk3ZLnTqkQ8130_assertion SIO_000772 10821226 NP284605.RAQg1AKhu9GWFC1L6Fs2H91rLSv2BnL25dbk3ZLnTqkQ8130_provenance.
- NP284605.RAQg1AKhu9GWFC1L6Fs2H91rLSv2BnL25dbk3ZLnTqkQ8130_assertion wasDerivedFrom befree-2016 NP284605.RAQg1AKhu9GWFC1L6Fs2H91rLSv2BnL25dbk3ZLnTqkQ8130_provenance.
- NP284605.RAQg1AKhu9GWFC1L6Fs2H91rLSv2BnL25dbk3ZLnTqkQ8130_assertion wasGeneratedBy ECO_0000203 NP284605.RAQg1AKhu9GWFC1L6Fs2H91rLSv2BnL25dbk3ZLnTqkQ8130_provenance.
- befree-2016 importedOn "2016-02-19" NP284605.RAQg1AKhu9GWFC1L6Fs2H91rLSv2BnL25dbk3ZLnTqkQ8130_provenance.