Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_provenance.
- 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.
- NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_assertion evidence source_evidence_literature NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_provenance.
- NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_assertion SIO_000772 22659343 NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_provenance.
- NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_assertion wasDerivedFrom befree-2016 NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_provenance.
- NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_assertion wasGeneratedBy ECO_0000203 NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_provenance.
- befree-2016 importedOn "2016-02-19" NP986664.RAUyWU0BUkUF5FwEYAxYOpsRuRfEdzHUhh4FCF9PdR5Q4130_provenance.