Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP740736.RAom2Y7Mqz1w5l6TTU82JnxFfqMxxwrQcKdYhvWeYmYR0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP740736.RAom2Y7Mqz1w5l6TTU82JnxFfqMxxwrQcKdYhvWeYmYR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP740736.RAom2Y7Mqz1w5l6TTU82JnxFfqMxxwrQcKdYhvWeYmYR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP740736.RAom2Y7Mqz1w5l6TTU82JnxFfqMxxwrQcKdYhvWeYmYR0130_provenance.
- NP740736.RAom2Y7Mqz1w5l6TTU82JnxFfqMxxwrQcKdYhvWeYmYR0130_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." NP740736.RAom2Y7Mqz1w5l6TTU82JnxFfqMxxwrQcKdYhvWeYmYR0130_provenance.
- NP740736.RAom2Y7Mqz1w5l6TTU82JnxFfqMxxwrQcKdYhvWeYmYR0130_assertion evidence source_evidence_literature NP740736.RAom2Y7Mqz1w5l6TTU82JnxFfqMxxwrQcKdYhvWeYmYR0130_provenance.
- NP740736.RAom2Y7Mqz1w5l6TTU82JnxFfqMxxwrQcKdYhvWeYmYR0130_assertion SIO_000772 19465477 NP740736.RAom2Y7Mqz1w5l6TTU82JnxFfqMxxwrQcKdYhvWeYmYR0130_provenance.
- NP740736.RAom2Y7Mqz1w5l6TTU82JnxFfqMxxwrQcKdYhvWeYmYR0130_assertion wasDerivedFrom befree-2016 NP740736.RAom2Y7Mqz1w5l6TTU82JnxFfqMxxwrQcKdYhvWeYmYR0130_provenance.
- NP740736.RAom2Y7Mqz1w5l6TTU82JnxFfqMxxwrQcKdYhvWeYmYR0130_assertion wasGeneratedBy ECO_0000203 NP740736.RAom2Y7Mqz1w5l6TTU82JnxFfqMxxwrQcKdYhvWeYmYR0130_provenance.
- befree-2016 importedOn "2016-02-19" NP740736.RAom2Y7Mqz1w5l6TTU82JnxFfqMxxwrQcKdYhvWeYmYR0130_provenance.