Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP570010.RAL4YrgHrr9ySsGDhl4BnjtsMZgX4Lj8qTwTzB_9p0Jio130_assertion> ?p ?o ?g. }
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- NP570010.RAL4YrgHrr9ySsGDhl4BnjtsMZgX4Lj8qTwTzB_9p0Jio130_assertion type Assertion NP570010.RAL4YrgHrr9ySsGDhl4BnjtsMZgX4Lj8qTwTzB_9p0Jio130_head.
- NP570010.RAL4YrgHrr9ySsGDhl4BnjtsMZgX4Lj8qTwTzB_9p0Jio130_assertion description "[Familial autosomal dominant frontotemporal dementia with ubiquitin-positive, tau-negative inclusions in the brain linked to 17q21-22 recently has been reported to carry null mutations in the progranulin gene (PGRN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570010.RAL4YrgHrr9ySsGDhl4BnjtsMZgX4Lj8qTwTzB_9p0Jio130_provenance.
- NP570010.RAL4YrgHrr9ySsGDhl4BnjtsMZgX4Lj8qTwTzB_9p0Jio130_assertion evidence source_evidence_literature NP570010.RAL4YrgHrr9ySsGDhl4BnjtsMZgX4Lj8qTwTzB_9p0Jio130_provenance.
- NP570010.RAL4YrgHrr9ySsGDhl4BnjtsMZgX4Lj8qTwTzB_9p0Jio130_assertion SIO_000772 16983685 NP570010.RAL4YrgHrr9ySsGDhl4BnjtsMZgX4Lj8qTwTzB_9p0Jio130_provenance.
- NP570010.RAL4YrgHrr9ySsGDhl4BnjtsMZgX4Lj8qTwTzB_9p0Jio130_assertion wasDerivedFrom befree-2016 NP570010.RAL4YrgHrr9ySsGDhl4BnjtsMZgX4Lj8qTwTzB_9p0Jio130_provenance.
- NP570010.RAL4YrgHrr9ySsGDhl4BnjtsMZgX4Lj8qTwTzB_9p0Jio130_assertion wasGeneratedBy ECO_0000203 NP570010.RAL4YrgHrr9ySsGDhl4BnjtsMZgX4Lj8qTwTzB_9p0Jio130_provenance.