Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP883186.RAHHsg-5OSbqWvSgRYh1OQIo8oW76AhZM0oo-B_XEJqLg130_assertion> ?p ?o ?g. }
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- NP883186.RAHHsg-5OSbqWvSgRYh1OQIo8oW76AhZM0oo-B_XEJqLg130_assertion type Assertion NP883186.RAHHsg-5OSbqWvSgRYh1OQIo8oW76AhZM0oo-B_XEJqLg130_head.
- NP883186.RAHHsg-5OSbqWvSgRYh1OQIo8oW76AhZM0oo-B_XEJqLg130_assertion wasGeneratedBy ECO_0000203 NP883186.RAHHsg-5OSbqWvSgRYh1OQIo8oW76AhZM0oo-B_XEJqLg130_provenance.
- NP883186.RAHHsg-5OSbqWvSgRYh1OQIo8oW76AhZM0oo-B_XEJqLg130_assertion wasDerivedFrom befree-20140225 NP883186.RAHHsg-5OSbqWvSgRYh1OQIo8oW76AhZM0oo-B_XEJqLg130_provenance.
- NP883186.RAHHsg-5OSbqWvSgRYh1OQIo8oW76AhZM0oo-B_XEJqLg130_assertion SIO_000772 19417767 NP883186.RAHHsg-5OSbqWvSgRYh1OQIo8oW76AhZM0oo-B_XEJqLg130_provenance.
- NP883186.RAHHsg-5OSbqWvSgRYh1OQIo8oW76AhZM0oo-B_XEJqLg130_assertion evidence source_evidence_literature NP883186.RAHHsg-5OSbqWvSgRYh1OQIo8oW76AhZM0oo-B_XEJqLg130_provenance.
- NP883186.RAHHsg-5OSbqWvSgRYh1OQIo8oW76AhZM0oo-B_XEJqLg130_assertion description "[We characterized a deletion distal to the DMRT genes in a patient with isolated 46,XY gonadal DSD and narrowed down the breakpoint in a patient with a 46,XY del(9)(p23) karyotype with gonadal DSD and mild symptoms of 9p deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883186.RAHHsg-5OSbqWvSgRYh1OQIo8oW76AhZM0oo-B_XEJqLg130_provenance.