Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP911034.RAsBgBO4_MfIzKvMsvhORyZ6NaDzrbb6GId2x5Orj6hC4130_assertion> ?p ?o ?g. }
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- NP911034.RAsBgBO4_MfIzKvMsvhORyZ6NaDzrbb6GId2x5Orj6hC4130_assertion type Assertion NP911034.RAsBgBO4_MfIzKvMsvhORyZ6NaDzrbb6GId2x5Orj6hC4130_head.
- NP911034.RAsBgBO4_MfIzKvMsvhORyZ6NaDzrbb6GId2x5Orj6hC4130_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." NP911034.RAsBgBO4_MfIzKvMsvhORyZ6NaDzrbb6GId2x5Orj6hC4130_provenance.
- NP911034.RAsBgBO4_MfIzKvMsvhORyZ6NaDzrbb6GId2x5Orj6hC4130_assertion evidence source_evidence_literature NP911034.RAsBgBO4_MfIzKvMsvhORyZ6NaDzrbb6GId2x5Orj6hC4130_provenance.
- NP911034.RAsBgBO4_MfIzKvMsvhORyZ6NaDzrbb6GId2x5Orj6hC4130_assertion SIO_000772 20593214 NP911034.RAsBgBO4_MfIzKvMsvhORyZ6NaDzrbb6GId2x5Orj6hC4130_provenance.
- NP911034.RAsBgBO4_MfIzKvMsvhORyZ6NaDzrbb6GId2x5Orj6hC4130_assertion wasDerivedFrom befree-20140225 NP911034.RAsBgBO4_MfIzKvMsvhORyZ6NaDzrbb6GId2x5Orj6hC4130_provenance.
- NP911034.RAsBgBO4_MfIzKvMsvhORyZ6NaDzrbb6GId2x5Orj6hC4130_assertion wasGeneratedBy ECO_0000203 NP911034.RAsBgBO4_MfIzKvMsvhORyZ6NaDzrbb6GId2x5Orj6hC4130_provenance.