Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP876654.RAVnF_jp52-MpZtb29a3oeh0ILN6hwRzLi2SbmTgVWkfM130_assertion> ?p ?o ?g. }
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- NP876654.RAVnF_jp52-MpZtb29a3oeh0ILN6hwRzLi2SbmTgVWkfM130_assertion type Assertion NP876654.RAVnF_jp52-MpZtb29a3oeh0ILN6hwRzLi2SbmTgVWkfM130_head.
- NP876654.RAVnF_jp52-MpZtb29a3oeh0ILN6hwRzLi2SbmTgVWkfM130_assertion description "[Although the frequency of the mutations is low in our series (4 of 188 patients [2%]), our results, similar to those already reported, support a direct pathogenic role of p62 in different types of FTD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP876654.RAVnF_jp52-MpZtb29a3oeh0ILN6hwRzLi2SbmTgVWkfM130_provenance.
- NP876654.RAVnF_jp52-MpZtb29a3oeh0ILN6hwRzLi2SbmTgVWkfM130_assertion evidence source_evidence_literature NP876654.RAVnF_jp52-MpZtb29a3oeh0ILN6hwRzLi2SbmTgVWkfM130_provenance.
- NP876654.RAVnF_jp52-MpZtb29a3oeh0ILN6hwRzLi2SbmTgVWkfM130_assertion SIO_000772 24042580 NP876654.RAVnF_jp52-MpZtb29a3oeh0ILN6hwRzLi2SbmTgVWkfM130_provenance.
- NP876654.RAVnF_jp52-MpZtb29a3oeh0ILN6hwRzLi2SbmTgVWkfM130_assertion wasDerivedFrom befree-20150227 NP876654.RAVnF_jp52-MpZtb29a3oeh0ILN6hwRzLi2SbmTgVWkfM130_provenance.
- NP876654.RAVnF_jp52-MpZtb29a3oeh0ILN6hwRzLi2SbmTgVWkfM130_assertion wasGeneratedBy ECO_0000203 NP876654.RAVnF_jp52-MpZtb29a3oeh0ILN6hwRzLi2SbmTgVWkfM130_provenance.