Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1249.RAkG5sJxPxuoWAR6YmO7jGahK9jmJBy-cXE2qVejGeVh4130_assertion> ?p ?o ?g. }
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- NP1249.RAkG5sJxPxuoWAR6YmO7jGahK9jmJBy-cXE2qVejGeVh4130_assertion type Assertion NP1249.RAkG5sJxPxuoWAR6YmO7jGahK9jmJBy-cXE2qVejGeVh4130_head.
- NP1249.RAkG5sJxPxuoWAR6YmO7jGahK9jmJBy-cXE2qVejGeVh4130_assertion wasGeneratedBy ECO_0000218 NP1249.RAkG5sJxPxuoWAR6YmO7jGahK9jmJBy-cXE2qVejGeVh4130_provenance.
- NP1249.RAkG5sJxPxuoWAR6YmO7jGahK9jmJBy-cXE2qVejGeVh4130_assertion wasDerivedFrom uniprot-20150221 NP1249.RAkG5sJxPxuoWAR6YmO7jGahK9jmJBy-cXE2qVejGeVh4130_provenance.
- NP1249.RAkG5sJxPxuoWAR6YmO7jGahK9jmJBy-cXE2qVejGeVh4130_assertion SIO_000772 9694901 NP1249.RAkG5sJxPxuoWAR6YmO7jGahK9jmJBy-cXE2qVejGeVh4130_provenance.
- NP1249.RAkG5sJxPxuoWAR6YmO7jGahK9jmJBy-cXE2qVejGeVh4130_assertion evidence source_evidence_curated NP1249.RAkG5sJxPxuoWAR6YmO7jGahK9jmJBy-cXE2qVejGeVh4130_provenance.
- NP1249.RAkG5sJxPxuoWAR6YmO7jGahK9jmJBy-cXE2qVejGeVh4130_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." NP1249.RAkG5sJxPxuoWAR6YmO7jGahK9jmJBy-cXE2qVejGeVh4130_provenance.