Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP184663.RASRTAtO_Hz9lzUC54s1Zf0q29Z0HrPjiosdWeFhzJBXQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP184663.RASRTAtO_Hz9lzUC54s1Zf0q29Z0HrPjiosdWeFhzJBXQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP184663.RASRTAtO_Hz9lzUC54s1Zf0q29Z0HrPjiosdWeFhzJBXQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP184663.RASRTAtO_Hz9lzUC54s1Zf0q29Z0HrPjiosdWeFhzJBXQ130_provenance.
- NP184663.RASRTAtO_Hz9lzUC54s1Zf0q29Z0HrPjiosdWeFhzJBXQ130_assertion description "[Non-amyloid, ubiquitinated cytoplasmic inclusions containing TDP-43 and its C-terminal fragments are pathological hallmarks of amyotrophic lateral sclerosis (ALS), a fatal motor neuron disorder, and frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184663.RASRTAtO_Hz9lzUC54s1Zf0q29Z0HrPjiosdWeFhzJBXQ130_provenance.
- NP184663.RASRTAtO_Hz9lzUC54s1Zf0q29Z0HrPjiosdWeFhzJBXQ130_assertion evidence source_evidence_literature NP184663.RASRTAtO_Hz9lzUC54s1Zf0q29Z0HrPjiosdWeFhzJBXQ130_provenance.
- NP184663.RASRTAtO_Hz9lzUC54s1Zf0q29Z0HrPjiosdWeFhzJBXQ130_assertion SIO_000772 19465477 NP184663.RASRTAtO_Hz9lzUC54s1Zf0q29Z0HrPjiosdWeFhzJBXQ130_provenance.
- NP184663.RASRTAtO_Hz9lzUC54s1Zf0q29Z0HrPjiosdWeFhzJBXQ130_assertion wasDerivedFrom befree-20140225 NP184663.RASRTAtO_Hz9lzUC54s1Zf0q29Z0HrPjiosdWeFhzJBXQ130_provenance.
- NP184663.RASRTAtO_Hz9lzUC54s1Zf0q29Z0HrPjiosdWeFhzJBXQ130_assertion wasGeneratedBy ECO_0000203 NP184663.RASRTAtO_Hz9lzUC54s1Zf0q29Z0HrPjiosdWeFhzJBXQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP184663.RASRTAtO_Hz9lzUC54s1Zf0q29Z0HrPjiosdWeFhzJBXQ130_provenance.