Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1070531.RAPUeMCP6TycbdOAfJRo13ejpBF4qbAS13nEpvA2bJAGU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1070531.RAPUeMCP6TycbdOAfJRo13ejpBF4qbAS13nEpvA2bJAGU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1070531.RAPUeMCP6TycbdOAfJRo13ejpBF4qbAS13nEpvA2bJAGU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1070531.RAPUeMCP6TycbdOAfJRo13ejpBF4qbAS13nEpvA2bJAGU130_provenance.
- NP1070531.RAPUeMCP6TycbdOAfJRo13ejpBF4qbAS13nEpvA2bJAGU130_assertion description "[The clinical presentation of the GRN A9D missense mutation is not restricted to behavioral variant frontotemporal dementia and may include aphasia, extrapyramidal features, and, notably, amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1070531.RAPUeMCP6TycbdOAfJRo13ejpBF4qbAS13nEpvA2bJAGU130_provenance.
- NP1070531.RAPUeMCP6TycbdOAfJRo13ejpBF4qbAS13nEpvA2bJAGU130_assertion evidence source_evidence_literature NP1070531.RAPUeMCP6TycbdOAfJRo13ejpBF4qbAS13nEpvA2bJAGU130_provenance.
- NP1070531.RAPUeMCP6TycbdOAfJRo13ejpBF4qbAS13nEpvA2bJAGU130_assertion SIO_000772 23596077 NP1070531.RAPUeMCP6TycbdOAfJRo13ejpBF4qbAS13nEpvA2bJAGU130_provenance.
- NP1070531.RAPUeMCP6TycbdOAfJRo13ejpBF4qbAS13nEpvA2bJAGU130_assertion wasDerivedFrom befree-2016 NP1070531.RAPUeMCP6TycbdOAfJRo13ejpBF4qbAS13nEpvA2bJAGU130_provenance.
- NP1070531.RAPUeMCP6TycbdOAfJRo13ejpBF4qbAS13nEpvA2bJAGU130_assertion wasGeneratedBy ECO_0000203 NP1070531.RAPUeMCP6TycbdOAfJRo13ejpBF4qbAS13nEpvA2bJAGU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1070531.RAPUeMCP6TycbdOAfJRo13ejpBF4qbAS13nEpvA2bJAGU130_provenance.