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- NP237189.RAw6jk4YX0FvHw9OMQ1PjLA1bVj1bO41KzOP8_JtS4HzE130_assertion type Assertion NP237189.RAw6jk4YX0FvHw9OMQ1PjLA1bVj1bO41KzOP8_JtS4HzE130_head.
- 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.
- NP237189.RAw6jk4YX0FvHw9OMQ1PjLA1bVj1bO41KzOP8_JtS4HzE130_assertion evidence source_evidence_literature NP237189.RAw6jk4YX0FvHw9OMQ1PjLA1bVj1bO41KzOP8_JtS4HzE130_provenance.
- NP237189.RAw6jk4YX0FvHw9OMQ1PjLA1bVj1bO41KzOP8_JtS4HzE130_assertion SIO_000772 18439221 NP237189.RAw6jk4YX0FvHw9OMQ1PjLA1bVj1bO41KzOP8_JtS4HzE130_provenance.
- NP237189.RAw6jk4YX0FvHw9OMQ1PjLA1bVj1bO41KzOP8_JtS4HzE130_assertion wasDerivedFrom lhgdn-20090331 NP237189.RAw6jk4YX0FvHw9OMQ1PjLA1bVj1bO41KzOP8_JtS4HzE130_provenance.
- NP237189.RAw6jk4YX0FvHw9OMQ1PjLA1bVj1bO41KzOP8_JtS4HzE130_assertion wasGeneratedBy ECO_0000203 NP237189.RAw6jk4YX0FvHw9OMQ1PjLA1bVj1bO41KzOP8_JtS4HzE130_provenance.