Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP919445.RAU9GsnflGKIbVzexQqGbusgVR3GMI0-eMQJHmpPQtpgU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP919445.RAU9GsnflGKIbVzexQqGbusgVR3GMI0-eMQJHmpPQtpgU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919445.RAU9GsnflGKIbVzexQqGbusgVR3GMI0-eMQJHmpPQtpgU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919445.RAU9GsnflGKIbVzexQqGbusgVR3GMI0-eMQJHmpPQtpgU130_provenance.
- NP919445.RAU9GsnflGKIbVzexQqGbusgVR3GMI0-eMQJHmpPQtpgU130_assertion description "[On the basis of the nature of the characteristic protein inclusions, frontotemporal lobar degeneration (FTLD) can be subdivided into the common FTLD-tau and FTLD-TDP as well as the less common FTLD-FUS and FTLD-UPS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919445.RAU9GsnflGKIbVzexQqGbusgVR3GMI0-eMQJHmpPQtpgU130_provenance.
- NP919445.RAU9GsnflGKIbVzexQqGbusgVR3GMI0-eMQJHmpPQtpgU130_assertion evidence source_evidence_literature NP919445.RAU9GsnflGKIbVzexQqGbusgVR3GMI0-eMQJHmpPQtpgU130_provenance.
- NP919445.RAU9GsnflGKIbVzexQqGbusgVR3GMI0-eMQJHmpPQtpgU130_assertion SIO_000772 22355793 NP919445.RAU9GsnflGKIbVzexQqGbusgVR3GMI0-eMQJHmpPQtpgU130_provenance.
- NP919445.RAU9GsnflGKIbVzexQqGbusgVR3GMI0-eMQJHmpPQtpgU130_assertion wasDerivedFrom befree-20140225 NP919445.RAU9GsnflGKIbVzexQqGbusgVR3GMI0-eMQJHmpPQtpgU130_provenance.
- NP919445.RAU9GsnflGKIbVzexQqGbusgVR3GMI0-eMQJHmpPQtpgU130_assertion wasGeneratedBy ECO_0000203 NP919445.RAU9GsnflGKIbVzexQqGbusgVR3GMI0-eMQJHmpPQtpgU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP919445.RAU9GsnflGKIbVzexQqGbusgVR3GMI0-eMQJHmpPQtpgU130_provenance.