Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP713002.RAuEbasC58MQg0GjKsF6TeZucKTKTzfn0zdE8xi3WJw9k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP713002.RAuEbasC58MQg0GjKsF6TeZucKTKTzfn0zdE8xi3WJw9k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP713002.RAuEbasC58MQg0GjKsF6TeZucKTKTzfn0zdE8xi3WJw9k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP713002.RAuEbasC58MQg0GjKsF6TeZucKTKTzfn0zdE8xi3WJw9k130_provenance.
- NP713002.RAuEbasC58MQg0GjKsF6TeZucKTKTzfn0zdE8xi3WJw9k130_assertion description "[Screening for mutations in the SRY gene in patients with mixed gonadal dysgenesis or with Turner syndrome and Y mosaicism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713002.RAuEbasC58MQg0GjKsF6TeZucKTKTzfn0zdE8xi3WJw9k130_provenance.
- NP713002.RAuEbasC58MQg0GjKsF6TeZucKTKTzfn0zdE8xi3WJw9k130_assertion evidence source_evidence_literature NP713002.RAuEbasC58MQg0GjKsF6TeZucKTKTzfn0zdE8xi3WJw9k130_provenance.
- NP713002.RAuEbasC58MQg0GjKsF6TeZucKTKTzfn0zdE8xi3WJw9k130_assertion SIO_000772 15223166 NP713002.RAuEbasC58MQg0GjKsF6TeZucKTKTzfn0zdE8xi3WJw9k130_provenance.
- NP713002.RAuEbasC58MQg0GjKsF6TeZucKTKTzfn0zdE8xi3WJw9k130_assertion wasDerivedFrom befree-20150227 NP713002.RAuEbasC58MQg0GjKsF6TeZucKTKTzfn0zdE8xi3WJw9k130_provenance.
- NP713002.RAuEbasC58MQg0GjKsF6TeZucKTKTzfn0zdE8xi3WJw9k130_assertion wasGeneratedBy ECO_0000203 NP713002.RAuEbasC58MQg0GjKsF6TeZucKTKTzfn0zdE8xi3WJw9k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP713002.RAuEbasC58MQg0GjKsF6TeZucKTKTzfn0zdE8xi3WJw9k130_provenance.