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- NP9835.RA6tiuvfDfWScTaVAsaPx-20G4PIT5aSo2sGFFck2fqDQ130_assertion type Assertion NP9835.RA6tiuvfDfWScTaVAsaPx-20G4PIT5aSo2sGFFck2fqDQ130_head.
- NP9835.RA6tiuvfDfWScTaVAsaPx-20G4PIT5aSo2sGFFck2fqDQ130_assertion wasGeneratedBy ECO_0000218 NP9835.RA6tiuvfDfWScTaVAsaPx-20G4PIT5aSo2sGFFck2fqDQ130_provenance.
- NP9835.RA6tiuvfDfWScTaVAsaPx-20G4PIT5aSo2sGFFck2fqDQ130_assertion wasDerivedFrom uniprot-2016 NP9835.RA6tiuvfDfWScTaVAsaPx-20G4PIT5aSo2sGFFck2fqDQ130_provenance.
- NP9835.RA6tiuvfDfWScTaVAsaPx-20G4PIT5aSo2sGFFck2fqDQ130_assertion SIO_000772 9694901 NP9835.RA6tiuvfDfWScTaVAsaPx-20G4PIT5aSo2sGFFck2fqDQ130_provenance.
- NP9835.RA6tiuvfDfWScTaVAsaPx-20G4PIT5aSo2sGFFck2fqDQ130_assertion evidence source_evidence_curated NP9835.RA6tiuvfDfWScTaVAsaPx-20G4PIT5aSo2sGFFck2fqDQ130_provenance.
- NP9835.RA6tiuvfDfWScTaVAsaPx-20G4PIT5aSo2sGFFck2fqDQ130_assertion description "[We have previously reported two sisters with chronic Sandhoff disease who were heterozygous for the common HEXB deletion allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9835.RA6tiuvfDfWScTaVAsaPx-20G4PIT5aSo2sGFFck2fqDQ130_provenance.