Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_assertion> ?p ?o ?g. }
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- NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_assertion type Assertion NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_head.
- NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_assertion description "[Recently, mutations in Progranulin (PGRN), predicted to cause premature truncation of the PGRN coding sequence, were found in patients with inherited FTLD-U and ub-ir neuronal intranuclear inclusions (NII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_provenance.
- NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_assertion evidence source_evidence_literature NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_provenance.
- NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_assertion SIO_000772 17202431 NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_provenance.
- NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_assertion wasDerivedFrom befree-2016 NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_provenance.
- NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_assertion wasGeneratedBy ECO_0000203 NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_provenance.