Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_provenance.
- NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_assertion description "[Mutations in chromosome X open reading frame 6 (CXorf6), a recently described candidate gene involved in the development of male genitalia, have been found in patients with complex 46,XY disorders of sexual development (46,XY DSD) including micropenis, bifid scrotum, and penoscrotal hypospadias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_provenance.
- NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_assertion evidence source_evidence_literature NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_provenance.
- NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_assertion SIO_000772 18635673 NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_provenance.
- NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_assertion wasDerivedFrom befree-20140225 NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_provenance.
- NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_assertion wasGeneratedBy ECO_0000203 NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_provenance.