Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4270.RAa2qre6ZdxYRQtW9x3RLGoMJCwhlFXmW9NUVCMxI8D1E130_assertion> ?p ?o ?g. }
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- NP4270.RAa2qre6ZdxYRQtW9x3RLGoMJCwhlFXmW9NUVCMxI8D1E130_assertion type Assertion NP4270.RAa2qre6ZdxYRQtW9x3RLGoMJCwhlFXmW9NUVCMxI8D1E130_head.
- NP4270.RAa2qre6ZdxYRQtW9x3RLGoMJCwhlFXmW9NUVCMxI8D1E130_assertion wasGeneratedBy ECO_0000218 NP4270.RAa2qre6ZdxYRQtW9x3RLGoMJCwhlFXmW9NUVCMxI8D1E130_provenance.
- NP4270.RAa2qre6ZdxYRQtW9x3RLGoMJCwhlFXmW9NUVCMxI8D1E130_assertion wasDerivedFrom uniprot-20130724 NP4270.RAa2qre6ZdxYRQtW9x3RLGoMJCwhlFXmW9NUVCMxI8D1E130_provenance.
- NP4270.RAa2qre6ZdxYRQtW9x3RLGoMJCwhlFXmW9NUVCMxI8D1E130_assertion SIO_000772 15821734 NP4270.RAa2qre6ZdxYRQtW9x3RLGoMJCwhlFXmW9NUVCMxI8D1E130_provenance.
- NP4270.RAa2qre6ZdxYRQtW9x3RLGoMJCwhlFXmW9NUVCMxI8D1E130_assertion evidence source_evidence_curated NP4270.RAa2qre6ZdxYRQtW9x3RLGoMJCwhlFXmW9NUVCMxI8D1E130_provenance.
- NP4270.RAa2qre6ZdxYRQtW9x3RLGoMJCwhlFXmW9NUVCMxI8D1E130_assertion description "[We show here that heterozygous mutations in the gene MYCN are present in Feingold syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4270.RAa2qre6ZdxYRQtW9x3RLGoMJCwhlFXmW9NUVCMxI8D1E130_provenance.