Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP512507.RAPdDFx8nEg0X4QVcBZzkcCeLoiej1r77LPuO-WnUHFo0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP512507.RAPdDFx8nEg0X4QVcBZzkcCeLoiej1r77LPuO-WnUHFo0130_assertion type Assertion NP512507.RAPdDFx8nEg0X4QVcBZzkcCeLoiej1r77LPuO-WnUHFo0130_head.
- NP512507.RAPdDFx8nEg0X4QVcBZzkcCeLoiej1r77LPuO-WnUHFo0130_assertion description "[PNFA, combined with limb apraxia was significantly more common in PGRN mutation cases than other FTLD cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512507.RAPdDFx8nEg0X4QVcBZzkcCeLoiej1r77LPuO-WnUHFo0130_provenance.
- NP512507.RAPdDFx8nEg0X4QVcBZzkcCeLoiej1r77LPuO-WnUHFo0130_assertion evidence source_evidence_literature NP512507.RAPdDFx8nEg0X4QVcBZzkcCeLoiej1r77LPuO-WnUHFo0130_provenance.
- NP512507.RAPdDFx8nEg0X4QVcBZzkcCeLoiej1r77LPuO-WnUHFo0130_assertion SIO_000772 18192287 NP512507.RAPdDFx8nEg0X4QVcBZzkcCeLoiej1r77LPuO-WnUHFo0130_provenance.
- NP512507.RAPdDFx8nEg0X4QVcBZzkcCeLoiej1r77LPuO-WnUHFo0130_assertion wasDerivedFrom befree-20140225 NP512507.RAPdDFx8nEg0X4QVcBZzkcCeLoiej1r77LPuO-WnUHFo0130_provenance.
- NP512507.RAPdDFx8nEg0X4QVcBZzkcCeLoiej1r77LPuO-WnUHFo0130_assertion wasGeneratedBy ECO_0000203 NP512507.RAPdDFx8nEg0X4QVcBZzkcCeLoiej1r77LPuO-WnUHFo0130_provenance.