Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP754392.RAzF-C10HOfr4AjSVp3tS3InrhMp3YbeMs8de0IvXV0iY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP754392.RAzF-C10HOfr4AjSVp3tS3InrhMp3YbeMs8de0IvXV0iY130_assertion type Assertion NP754392.RAzF-C10HOfr4AjSVp3tS3InrhMp3YbeMs8de0IvXV0iY130_head.
- NP754392.RAzF-C10HOfr4AjSVp3tS3InrhMp3YbeMs8de0IvXV0iY130_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." NP754392.RAzF-C10HOfr4AjSVp3tS3InrhMp3YbeMs8de0IvXV0iY130_provenance.
- NP754392.RAzF-C10HOfr4AjSVp3tS3InrhMp3YbeMs8de0IvXV0iY130_assertion evidence source_evidence_literature NP754392.RAzF-C10HOfr4AjSVp3tS3InrhMp3YbeMs8de0IvXV0iY130_provenance.
- NP754392.RAzF-C10HOfr4AjSVp3tS3InrhMp3YbeMs8de0IvXV0iY130_assertion SIO_000772 7565304 NP754392.RAzF-C10HOfr4AjSVp3tS3InrhMp3YbeMs8de0IvXV0iY130_provenance.
- NP754392.RAzF-C10HOfr4AjSVp3tS3InrhMp3YbeMs8de0IvXV0iY130_assertion wasDerivedFrom befree-20150227 NP754392.RAzF-C10HOfr4AjSVp3tS3InrhMp3YbeMs8de0IvXV0iY130_provenance.
- NP754392.RAzF-C10HOfr4AjSVp3tS3InrhMp3YbeMs8de0IvXV0iY130_assertion wasGeneratedBy ECO_0000203 NP754392.RAzF-C10HOfr4AjSVp3tS3InrhMp3YbeMs8de0IvXV0iY130_provenance.