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- NP660570.RAukgS1jUwQXyrCld0tXmwrTsu3IomxIvDvD_InkTQSWU130_assertion type Assertion NP660570.RAukgS1jUwQXyrCld0tXmwrTsu3IomxIvDvD_InkTQSWU130_head.
- NP660570.RAukgS1jUwQXyrCld0tXmwrTsu3IomxIvDvD_InkTQSWU130_assertion description "[We also report a germline PHOX2B mutation in one patient treated for Hirschsprung's disease who subsequently developed a multifocal neuroblastoma in infancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660570.RAukgS1jUwQXyrCld0tXmwrTsu3IomxIvDvD_InkTQSWU130_provenance.
- NP660570.RAukgS1jUwQXyrCld0tXmwrTsu3IomxIvDvD_InkTQSWU130_assertion evidence source_evidence_literature NP660570.RAukgS1jUwQXyrCld0tXmwrTsu3IomxIvDvD_InkTQSWU130_provenance.
- NP660570.RAukgS1jUwQXyrCld0tXmwrTsu3IomxIvDvD_InkTQSWU130_assertion SIO_000772 15949893 NP660570.RAukgS1jUwQXyrCld0tXmwrTsu3IomxIvDvD_InkTQSWU130_provenance.
- NP660570.RAukgS1jUwQXyrCld0tXmwrTsu3IomxIvDvD_InkTQSWU130_assertion wasDerivedFrom befree-20140225 NP660570.RAukgS1jUwQXyrCld0tXmwrTsu3IomxIvDvD_InkTQSWU130_provenance.
- NP660570.RAukgS1jUwQXyrCld0tXmwrTsu3IomxIvDvD_InkTQSWU130_assertion wasGeneratedBy ECO_0000203 NP660570.RAukgS1jUwQXyrCld0tXmwrTsu3IomxIvDvD_InkTQSWU130_provenance.