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- source_evidence_literature type ECO_0000212 NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP587110.RAuITGOaL5j-xnxm-OaIzs41g3n7SW937qeh91kZrXWeo130_provenance.