Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP766349.RAx09MJ5e5FzVoQzaDfB0ZntSklPK8aBX2SZEbYzvmCC0130_assertion> ?p ?o ?g. }
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- NP766349.RAx09MJ5e5FzVoQzaDfB0ZntSklPK8aBX2SZEbYzvmCC0130_assertion type Assertion NP766349.RAx09MJ5e5FzVoQzaDfB0ZntSklPK8aBX2SZEbYzvmCC0130_head.
- NP766349.RAx09MJ5e5FzVoQzaDfB0ZntSklPK8aBX2SZEbYzvmCC0130_assertion wasGeneratedBy ECO_0000203 NP766349.RAx09MJ5e5FzVoQzaDfB0ZntSklPK8aBX2SZEbYzvmCC0130_provenance.
- NP766349.RAx09MJ5e5FzVoQzaDfB0ZntSklPK8aBX2SZEbYzvmCC0130_assertion wasDerivedFrom befree-2016 NP766349.RAx09MJ5e5FzVoQzaDfB0ZntSklPK8aBX2SZEbYzvmCC0130_provenance.
- NP766349.RAx09MJ5e5FzVoQzaDfB0ZntSklPK8aBX2SZEbYzvmCC0130_assertion SIO_000772 1979048 NP766349.RAx09MJ5e5FzVoQzaDfB0ZntSklPK8aBX2SZEbYzvmCC0130_provenance.
- NP766349.RAx09MJ5e5FzVoQzaDfB0ZntSklPK8aBX2SZEbYzvmCC0130_assertion evidence source_evidence_literature NP766349.RAx09MJ5e5FzVoQzaDfB0ZntSklPK8aBX2SZEbYzvmCC0130_provenance.
- NP766349.RAx09MJ5e5FzVoQzaDfB0ZntSklPK8aBX2SZEbYzvmCC0130_assertion description "[Two independent familial STS deletions, one of which is associated with a phenotype of ichthyosis plus ocular albinism (XI/OA1) and the other with nystagmus plus Rud syndrome, lack some but not all of the normal S232 PFGE fragments.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766349.RAx09MJ5e5FzVoQzaDfB0ZntSklPK8aBX2SZEbYzvmCC0130_provenance.