Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP213813.RATfCWakjzGtnDcB1Ohgwc3c0VGTPMfFaAsNwuzRVFBLk130_assertion> ?p ?o ?g. }
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- NP213813.RATfCWakjzGtnDcB1Ohgwc3c0VGTPMfFaAsNwuzRVFBLk130_assertion type Assertion NP213813.RATfCWakjzGtnDcB1Ohgwc3c0VGTPMfFaAsNwuzRVFBLk130_head.
- NP213813.RATfCWakjzGtnDcB1Ohgwc3c0VGTPMfFaAsNwuzRVFBLk130_assertion wasGeneratedBy ECO_0000203 NP213813.RATfCWakjzGtnDcB1Ohgwc3c0VGTPMfFaAsNwuzRVFBLk130_provenance.
- NP213813.RATfCWakjzGtnDcB1Ohgwc3c0VGTPMfFaAsNwuzRVFBLk130_assertion wasDerivedFrom befree-20140225 NP213813.RATfCWakjzGtnDcB1Ohgwc3c0VGTPMfFaAsNwuzRVFBLk130_provenance.
- NP213813.RATfCWakjzGtnDcB1Ohgwc3c0VGTPMfFaAsNwuzRVFBLk130_assertion SIO_000772 7902323 NP213813.RATfCWakjzGtnDcB1Ohgwc3c0VGTPMfFaAsNwuzRVFBLk130_provenance.
- NP213813.RATfCWakjzGtnDcB1Ohgwc3c0VGTPMfFaAsNwuzRVFBLk130_assertion evidence source_evidence_literature NP213813.RATfCWakjzGtnDcB1Ohgwc3c0VGTPMfFaAsNwuzRVFBLk130_provenance.
- NP213813.RATfCWakjzGtnDcB1Ohgwc3c0VGTPMfFaAsNwuzRVFBLk130_assertion description "[The exclusion of linkage 15 cM on each side of PAH in 16 families with MJD shows that these two forms of dominant ataxia are genetically distinct and at different chromosomal locations (nonallelic).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213813.RATfCWakjzGtnDcB1Ohgwc3c0VGTPMfFaAsNwuzRVFBLk130_provenance.