Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP458742.RA88N9dDRTFSNXnNJ0kfXi0k5q0Znmm3NSrAyFGY9Dwyc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP458742.RA88N9dDRTFSNXnNJ0kfXi0k5q0Znmm3NSrAyFGY9Dwyc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP458742.RA88N9dDRTFSNXnNJ0kfXi0k5q0Znmm3NSrAyFGY9Dwyc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP458742.RA88N9dDRTFSNXnNJ0kfXi0k5q0Znmm3NSrAyFGY9Dwyc130_provenance.
- NP458742.RA88N9dDRTFSNXnNJ0kfXi0k5q0Znmm3NSrAyFGY9Dwyc130_assertion wasGeneratedBy ECO_0000203 NP458742.RA88N9dDRTFSNXnNJ0kfXi0k5q0Znmm3NSrAyFGY9Dwyc130_provenance.
- NP458742.RA88N9dDRTFSNXnNJ0kfXi0k5q0Znmm3NSrAyFGY9Dwyc130_assertion wasDerivedFrom befree-20140225 NP458742.RA88N9dDRTFSNXnNJ0kfXi0k5q0Znmm3NSrAyFGY9Dwyc130_provenance.
- NP458742.RA88N9dDRTFSNXnNJ0kfXi0k5q0Znmm3NSrAyFGY9Dwyc130_assertion SIO_000772 17030535 NP458742.RA88N9dDRTFSNXnNJ0kfXi0k5q0Znmm3NSrAyFGY9Dwyc130_provenance.
- NP458742.RA88N9dDRTFSNXnNJ0kfXi0k5q0Znmm3NSrAyFGY9Dwyc130_assertion evidence source_evidence_literature NP458742.RA88N9dDRTFSNXnNJ0kfXi0k5q0Znmm3NSrAyFGY9Dwyc130_provenance.
- NP458742.RA88N9dDRTFSNXnNJ0kfXi0k5q0Znmm3NSrAyFGY9Dwyc130_assertion description "[These findings suggest that the insR352 PSEN1 is not pathogenic, and the IVS1+1G-->A mutation in PGRN causes FTDP associated with FTLD-U pathology and represents a new class of neurodegenerative disease--the 'hypoprogranulinopathies'.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP458742.RA88N9dDRTFSNXnNJ0kfXi0k5q0Znmm3NSrAyFGY9Dwyc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP458742.RA88N9dDRTFSNXnNJ0kfXi0k5q0Znmm3NSrAyFGY9Dwyc130_provenance.