Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP126780.RA8LzIrGMxOuPXKZC4AzQz3_auOvYfi9XU59Xz3cHV6kw130_assertion> ?p ?o ?g. }
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- NP126780.RA8LzIrGMxOuPXKZC4AzQz3_auOvYfi9XU59Xz3cHV6kw130_assertion type Assertion NP126780.RA8LzIrGMxOuPXKZC4AzQz3_auOvYfi9XU59Xz3cHV6kw130_head.
- 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.
- NP126780.RA8LzIrGMxOuPXKZC4AzQz3_auOvYfi9XU59Xz3cHV6kw130_assertion evidence source_evidence_literature NP126780.RA8LzIrGMxOuPXKZC4AzQz3_auOvYfi9XU59Xz3cHV6kw130_provenance.
- NP126780.RA8LzIrGMxOuPXKZC4AzQz3_auOvYfi9XU59Xz3cHV6kw130_assertion SIO_000772 18439221 NP126780.RA8LzIrGMxOuPXKZC4AzQz3_auOvYfi9XU59Xz3cHV6kw130_provenance.
- NP126780.RA8LzIrGMxOuPXKZC4AzQz3_auOvYfi9XU59Xz3cHV6kw130_assertion wasDerivedFrom lhgdn-20090331 NP126780.RA8LzIrGMxOuPXKZC4AzQz3_auOvYfi9XU59Xz3cHV6kw130_provenance.
- NP126780.RA8LzIrGMxOuPXKZC4AzQz3_auOvYfi9XU59Xz3cHV6kw130_assertion wasGeneratedBy ECO_0000203 NP126780.RA8LzIrGMxOuPXKZC4AzQz3_auOvYfi9XU59Xz3cHV6kw130_provenance.