Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP877499.RAzgHmkEe9dVRVZojbxI-GpG1bdhS4gdB4muHYxPhQ8Pg130_assertion> ?p ?o ?g. }
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- NP877499.RAzgHmkEe9dVRVZojbxI-GpG1bdhS4gdB4muHYxPhQ8Pg130_assertion type Assertion NP877499.RAzgHmkEe9dVRVZojbxI-GpG1bdhS4gdB4muHYxPhQ8Pg130_head.
- NP877499.RAzgHmkEe9dVRVZojbxI-GpG1bdhS4gdB4muHYxPhQ8Pg130_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." NP877499.RAzgHmkEe9dVRVZojbxI-GpG1bdhS4gdB4muHYxPhQ8Pg130_provenance.
- NP877499.RAzgHmkEe9dVRVZojbxI-GpG1bdhS4gdB4muHYxPhQ8Pg130_assertion evidence source_evidence_literature NP877499.RAzgHmkEe9dVRVZojbxI-GpG1bdhS4gdB4muHYxPhQ8Pg130_provenance.
- NP877499.RAzgHmkEe9dVRVZojbxI-GpG1bdhS4gdB4muHYxPhQ8Pg130_assertion SIO_000772 15949893 NP877499.RAzgHmkEe9dVRVZojbxI-GpG1bdhS4gdB4muHYxPhQ8Pg130_provenance.
- NP877499.RAzgHmkEe9dVRVZojbxI-GpG1bdhS4gdB4muHYxPhQ8Pg130_assertion wasDerivedFrom befree-20140225 NP877499.RAzgHmkEe9dVRVZojbxI-GpG1bdhS4gdB4muHYxPhQ8Pg130_provenance.
- NP877499.RAzgHmkEe9dVRVZojbxI-GpG1bdhS4gdB4muHYxPhQ8Pg130_assertion wasGeneratedBy ECO_0000203 NP877499.RAzgHmkEe9dVRVZojbxI-GpG1bdhS4gdB4muHYxPhQ8Pg130_provenance.