Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_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." NP110964.RAm0wKzc8AqrQ3TVEPPbQuUoKb99ECJROwM43Y4izUcTo130_provenance.
- NP153779.RAmNMfafJnz4GQYOa6aFlhPjTKVod13qggqhgkgVJXjpg130_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." NP153779.RAmNMfafJnz4GQYOa6aFlhPjTKVod13qggqhgkgVJXjpg130_provenance.
- 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." provenance.
- 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." provenance.
- NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_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." NP220319.RAv9JGah7FmbSVKUrGe3CRrwMyAeO8D4HH_23W6KJO4i0130_provenance.
- NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_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." NP174176.RAJo52DagS-eOMp2FGLQhdU7QlaT-r71KSWbjrpKvHWMI130_provenance.
- 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.
- NP220320.RAIX7twvDqDpU_BQrSCCFxIKjNEO4ryead2qNjlt1JGJ8130_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." NP220320.RAIX7twvDqDpU_BQrSCCFxIKjNEO4ryead2qNjlt1JGJ8130_provenance.