Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP216886.RAJi2aaDeKcMe9zFQw_wWlAgPdhsFeDzpc4_xUROzy0oU130_assertion> ?p ?o ?g. }
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- NP216886.RAJi2aaDeKcMe9zFQw_wWlAgPdhsFeDzpc4_xUROzy0oU130_assertion type Assertion NP216886.RAJi2aaDeKcMe9zFQw_wWlAgPdhsFeDzpc4_xUROzy0oU130_head.
- NP216886.RAJi2aaDeKcMe9zFQw_wWlAgPdhsFeDzpc4_xUROzy0oU130_assertion description "[2 patients whose clinical features resembled those of multiple system atrophy of the cerebellar subtype (MSA-C) but without ocular motor apraxia and hypoalbuminemia/had a different nucleotide transition in the APTX gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216886.RAJi2aaDeKcMe9zFQw_wWlAgPdhsFeDzpc4_xUROzy0oU130_provenance.
- NP216886.RAJi2aaDeKcMe9zFQw_wWlAgPdhsFeDzpc4_xUROzy0oU130_assertion evidence source_evidence_literature NP216886.RAJi2aaDeKcMe9zFQw_wWlAgPdhsFeDzpc4_xUROzy0oU130_provenance.
- NP216886.RAJi2aaDeKcMe9zFQw_wWlAgPdhsFeDzpc4_xUROzy0oU130_assertion SIO_000772 17049295 NP216886.RAJi2aaDeKcMe9zFQw_wWlAgPdhsFeDzpc4_xUROzy0oU130_provenance.
- NP216886.RAJi2aaDeKcMe9zFQw_wWlAgPdhsFeDzpc4_xUROzy0oU130_assertion wasDerivedFrom lhgdn-20090331 NP216886.RAJi2aaDeKcMe9zFQw_wWlAgPdhsFeDzpc4_xUROzy0oU130_provenance.
- NP216886.RAJi2aaDeKcMe9zFQw_wWlAgPdhsFeDzpc4_xUROzy0oU130_assertion wasGeneratedBy ECO_0000203 NP216886.RAJi2aaDeKcMe9zFQw_wWlAgPdhsFeDzpc4_xUROzy0oU130_provenance.