Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP895413.RAXgUubLwiyUF7oGGcMiTHuvQFPTslpOvgm6yOJKOK1y4130_assertion> ?p ?o ?g. }
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- NP895413.RAXgUubLwiyUF7oGGcMiTHuvQFPTslpOvgm6yOJKOK1y4130_assertion type Assertion NP895413.RAXgUubLwiyUF7oGGcMiTHuvQFPTslpOvgm6yOJKOK1y4130_head.
- NP895413.RAXgUubLwiyUF7oGGcMiTHuvQFPTslpOvgm6yOJKOK1y4130_assertion description "[Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895413.RAXgUubLwiyUF7oGGcMiTHuvQFPTslpOvgm6yOJKOK1y4130_provenance.
- NP895413.RAXgUubLwiyUF7oGGcMiTHuvQFPTslpOvgm6yOJKOK1y4130_assertion evidence source_evidence_literature NP895413.RAXgUubLwiyUF7oGGcMiTHuvQFPTslpOvgm6yOJKOK1y4130_provenance.
- NP895413.RAXgUubLwiyUF7oGGcMiTHuvQFPTslpOvgm6yOJKOK1y4130_assertion SIO_000772 22169395 NP895413.RAXgUubLwiyUF7oGGcMiTHuvQFPTslpOvgm6yOJKOK1y4130_provenance.
- NP895413.RAXgUubLwiyUF7oGGcMiTHuvQFPTslpOvgm6yOJKOK1y4130_assertion wasDerivedFrom befree-20150227 NP895413.RAXgUubLwiyUF7oGGcMiTHuvQFPTslpOvgm6yOJKOK1y4130_provenance.
- NP895413.RAXgUubLwiyUF7oGGcMiTHuvQFPTslpOvgm6yOJKOK1y4130_assertion wasGeneratedBy ECO_0000203 NP895413.RAXgUubLwiyUF7oGGcMiTHuvQFPTslpOvgm6yOJKOK1y4130_provenance.