Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1111434.RAAP3VEnSgiukdeSOxfHapS9OMKvAa5s3k8tPUeq_8_sI130_assertion> ?p ?o ?g. }
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- NP1111434.RAAP3VEnSgiukdeSOxfHapS9OMKvAa5s3k8tPUeq_8_sI130_assertion type Assertion NP1111434.RAAP3VEnSgiukdeSOxfHapS9OMKvAa5s3k8tPUeq_8_sI130_head.
- NP1111434.RAAP3VEnSgiukdeSOxfHapS9OMKvAa5s3k8tPUeq_8_sI130_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." NP1111434.RAAP3VEnSgiukdeSOxfHapS9OMKvAa5s3k8tPUeq_8_sI130_provenance.
- NP1111434.RAAP3VEnSgiukdeSOxfHapS9OMKvAa5s3k8tPUeq_8_sI130_assertion evidence source_evidence_literature NP1111434.RAAP3VEnSgiukdeSOxfHapS9OMKvAa5s3k8tPUeq_8_sI130_provenance.
- NP1111434.RAAP3VEnSgiukdeSOxfHapS9OMKvAa5s3k8tPUeq_8_sI130_assertion SIO_000772 24042580 NP1111434.RAAP3VEnSgiukdeSOxfHapS9OMKvAa5s3k8tPUeq_8_sI130_provenance.
- NP1111434.RAAP3VEnSgiukdeSOxfHapS9OMKvAa5s3k8tPUeq_8_sI130_assertion wasDerivedFrom befree-2016 NP1111434.RAAP3VEnSgiukdeSOxfHapS9OMKvAa5s3k8tPUeq_8_sI130_provenance.
- NP1111434.RAAP3VEnSgiukdeSOxfHapS9OMKvAa5s3k8tPUeq_8_sI130_assertion wasGeneratedBy ECO_0000203 NP1111434.RAAP3VEnSgiukdeSOxfHapS9OMKvAa5s3k8tPUeq_8_sI130_provenance.