Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP478825.RAbE4vZuJVVGeV4vecBnRrIzYJW_RyeRou-vVJ4teuxeI130_assertion> ?p ?o ?g. }
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- NP478825.RAbE4vZuJVVGeV4vecBnRrIzYJW_RyeRou-vVJ4teuxeI130_assertion type Assertion NP478825.RAbE4vZuJVVGeV4vecBnRrIzYJW_RyeRou-vVJ4teuxeI130_head.
- NP478825.RAbE4vZuJVVGeV4vecBnRrIzYJW_RyeRou-vVJ4teuxeI130_assertion description "[These data are consistent with earlier findings that p53 mutations are rare in PNETs, which are primarily pediatric tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478825.RAbE4vZuJVVGeV4vecBnRrIzYJW_RyeRou-vVJ4teuxeI130_provenance.
- NP478825.RAbE4vZuJVVGeV4vecBnRrIzYJW_RyeRou-vVJ4teuxeI130_assertion evidence source_evidence_literature NP478825.RAbE4vZuJVVGeV4vecBnRrIzYJW_RyeRou-vVJ4teuxeI130_provenance.
- NP478825.RAbE4vZuJVVGeV4vecBnRrIzYJW_RyeRou-vVJ4teuxeI130_assertion SIO_000772 7565304 NP478825.RAbE4vZuJVVGeV4vecBnRrIzYJW_RyeRou-vVJ4teuxeI130_provenance.
- NP478825.RAbE4vZuJVVGeV4vecBnRrIzYJW_RyeRou-vVJ4teuxeI130_assertion wasDerivedFrom befree-20140225 NP478825.RAbE4vZuJVVGeV4vecBnRrIzYJW_RyeRou-vVJ4teuxeI130_provenance.
- NP478825.RAbE4vZuJVVGeV4vecBnRrIzYJW_RyeRou-vVJ4teuxeI130_assertion wasGeneratedBy ECO_0000203 NP478825.RAbE4vZuJVVGeV4vecBnRrIzYJW_RyeRou-vVJ4teuxeI130_provenance.