Matches in Nanopublications for { ?s ?p "[SPG11 mutations should be suspected in patients with isolated or recessive HSP, thin corpus callosum and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 4 of
4
with 100 items per page.
- NP126780.RA8LzIrGMxOuPXKZC4AzQz3_auOvYfi9XU59Xz3cHV6kw130_assertion description "[SPG11 mutations should be suspected in patients with isolated or recessive HSP, thin corpus callosum and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP126780.RA8LzIrGMxOuPXKZC4AzQz3_auOvYfi9XU59Xz3cHV6kw130_provenance.
- assertion description "[SPG11 mutations should be suspected in patients with isolated or recessive HSP, thin corpus callosum and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_assertion description "[SPG11 mutations should be suspected in patients with isolated or recessive HSP, thin corpus callosum and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_provenance.
- NP237189.RAw6jk4YX0FvHw9OMQ1PjLA1bVj1bO41KzOP8_JtS4HzE130_assertion description "[SPG11 mutations should be suspected in patients with isolated or recessive HSP, thin corpus callosum and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237189.RAw6jk4YX0FvHw9OMQ1PjLA1bVj1bO41KzOP8_JtS4HzE130_provenance.