Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_assertion> ?p ?o ?g. }
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- NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_assertion type Assertion NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_head.
- NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_assertion description "[We retrospectively reviewed genome wide array-CGH data in order to determine the frequency and nature of chromosome X-copy number variations (X-CNV) in a cohort of 2222 sporadic male patients with intellectual disability (ID) referred to us for diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_provenance.
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- NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_assertion wasDerivedFrom befree-2016 NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_provenance.
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