Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP582743.RAa3Lf08AWpkMVdJ0hIcPxIQhsW5pMAY7uvTzleulnm4o130_assertion> ?p ?o ?g. }
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- NP582743.RAa3Lf08AWpkMVdJ0hIcPxIQhsW5pMAY7uvTzleulnm4o130_assertion type Assertion NP582743.RAa3Lf08AWpkMVdJ0hIcPxIQhsW5pMAY7uvTzleulnm4o130_head.
- NP582743.RAa3Lf08AWpkMVdJ0hIcPxIQhsW5pMAY7uvTzleulnm4o130_assertion description "[We have used comparative genomic hybridization to identify genome copy number changes that can predict outcome in patients with stage IV neuroblastoma without MYCN amplification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582743.RAa3Lf08AWpkMVdJ0hIcPxIQhsW5pMAY7uvTzleulnm4o130_provenance.
- NP582743.RAa3Lf08AWpkMVdJ0hIcPxIQhsW5pMAY7uvTzleulnm4o130_assertion evidence source_evidence_literature NP582743.RAa3Lf08AWpkMVdJ0hIcPxIQhsW5pMAY7uvTzleulnm4o130_provenance.
- NP582743.RAa3Lf08AWpkMVdJ0hIcPxIQhsW5pMAY7uvTzleulnm4o130_assertion SIO_000772 18765546 NP582743.RAa3Lf08AWpkMVdJ0hIcPxIQhsW5pMAY7uvTzleulnm4o130_provenance.
- NP582743.RAa3Lf08AWpkMVdJ0hIcPxIQhsW5pMAY7uvTzleulnm4o130_assertion wasDerivedFrom befree-20150227 NP582743.RAa3Lf08AWpkMVdJ0hIcPxIQhsW5pMAY7uvTzleulnm4o130_provenance.
- NP582743.RAa3Lf08AWpkMVdJ0hIcPxIQhsW5pMAY7uvTzleulnm4o130_assertion wasGeneratedBy ECO_0000203 NP582743.RAa3Lf08AWpkMVdJ0hIcPxIQhsW5pMAY7uvTzleulnm4o130_provenance.