Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP932990.RArMiC0XFRza17e0CrhEniKQnnOdpYuO5ItnQEdjTaSnI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP932990.RArMiC0XFRza17e0CrhEniKQnnOdpYuO5ItnQEdjTaSnI130_assertion type Assertion NP932990.RArMiC0XFRza17e0CrhEniKQnnOdpYuO5ItnQEdjTaSnI130_head.
- NP932990.RArMiC0XFRza17e0CrhEniKQnnOdpYuO5ItnQEdjTaSnI130_assertion description "[A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932990.RArMiC0XFRza17e0CrhEniKQnnOdpYuO5ItnQEdjTaSnI130_provenance.
- NP932990.RArMiC0XFRza17e0CrhEniKQnnOdpYuO5ItnQEdjTaSnI130_assertion evidence source_evidence_literature NP932990.RArMiC0XFRza17e0CrhEniKQnnOdpYuO5ItnQEdjTaSnI130_provenance.
- NP932990.RArMiC0XFRza17e0CrhEniKQnnOdpYuO5ItnQEdjTaSnI130_assertion SIO_000772 20593214 NP932990.RArMiC0XFRza17e0CrhEniKQnnOdpYuO5ItnQEdjTaSnI130_provenance.
- NP932990.RArMiC0XFRza17e0CrhEniKQnnOdpYuO5ItnQEdjTaSnI130_assertion wasDerivedFrom befree-20150227 NP932990.RArMiC0XFRza17e0CrhEniKQnnOdpYuO5ItnQEdjTaSnI130_provenance.
- NP932990.RArMiC0XFRza17e0CrhEniKQnnOdpYuO5ItnQEdjTaSnI130_assertion wasGeneratedBy ECO_0000203 NP932990.RArMiC0XFRza17e0CrhEniKQnnOdpYuO5ItnQEdjTaSnI130_provenance.