Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP550972.RAbvTtxnMiCgtsJ0h2xAJN_hUaskO2JdWL9X8jcEf6CYU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP550972.RAbvTtxnMiCgtsJ0h2xAJN_hUaskO2JdWL9X8jcEf6CYU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP550972.RAbvTtxnMiCgtsJ0h2xAJN_hUaskO2JdWL9X8jcEf6CYU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP550972.RAbvTtxnMiCgtsJ0h2xAJN_hUaskO2JdWL9X8jcEf6CYU130_provenance.
- NP550972.RAbvTtxnMiCgtsJ0h2xAJN_hUaskO2JdWL9X8jcEf6CYU130_assertion description "[Biofluid studies identify about 15% of patients with FTLD due to a genetic mutation that is associated with the specific histopathologic features of TDP-43 or a tauopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP550972.RAbvTtxnMiCgtsJ0h2xAJN_hUaskO2JdWL9X8jcEf6CYU130_provenance.
- NP550972.RAbvTtxnMiCgtsJ0h2xAJN_hUaskO2JdWL9X8jcEf6CYU130_assertion evidence source_evidence_literature NP550972.RAbvTtxnMiCgtsJ0h2xAJN_hUaskO2JdWL9X8jcEf6CYU130_provenance.
- NP550972.RAbvTtxnMiCgtsJ0h2xAJN_hUaskO2JdWL9X8jcEf6CYU130_assertion SIO_000772 20881489 NP550972.RAbvTtxnMiCgtsJ0h2xAJN_hUaskO2JdWL9X8jcEf6CYU130_provenance.
- NP550972.RAbvTtxnMiCgtsJ0h2xAJN_hUaskO2JdWL9X8jcEf6CYU130_assertion wasDerivedFrom befree-20140225 NP550972.RAbvTtxnMiCgtsJ0h2xAJN_hUaskO2JdWL9X8jcEf6CYU130_provenance.
- NP550972.RAbvTtxnMiCgtsJ0h2xAJN_hUaskO2JdWL9X8jcEf6CYU130_assertion wasGeneratedBy ECO_0000203 NP550972.RAbvTtxnMiCgtsJ0h2xAJN_hUaskO2JdWL9X8jcEf6CYU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP550972.RAbvTtxnMiCgtsJ0h2xAJN_hUaskO2JdWL9X8jcEf6CYU130_provenance.