Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP691139.RA_Ug6NFaqzT4ugdNLcjH1XkB1WlUwYuVQJ7g4ccZuMxw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP691139.RA_Ug6NFaqzT4ugdNLcjH1XkB1WlUwYuVQJ7g4ccZuMxw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691139.RA_Ug6NFaqzT4ugdNLcjH1XkB1WlUwYuVQJ7g4ccZuMxw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691139.RA_Ug6NFaqzT4ugdNLcjH1XkB1WlUwYuVQJ7g4ccZuMxw130_provenance.
- NP691139.RA_Ug6NFaqzT4ugdNLcjH1XkB1WlUwYuVQJ7g4ccZuMxw130_assertion description "[These models express G37R mutant Cu/Zn superoxide dismutase (SOD1G37R; fALS), A53T mutant alpha-synuclein (alpha-SynA53T; PD), full-length mutant atrophin-1-65Q, and htt-N171-82Q (huntingtin N-terminal fragment; HD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691139.RA_Ug6NFaqzT4ugdNLcjH1XkB1WlUwYuVQJ7g4ccZuMxw130_provenance.
- NP691139.RA_Ug6NFaqzT4ugdNLcjH1XkB1WlUwYuVQJ7g4ccZuMxw130_assertion evidence source_evidence_literature NP691139.RA_Ug6NFaqzT4ugdNLcjH1XkB1WlUwYuVQJ7g4ccZuMxw130_provenance.
- NP691139.RA_Ug6NFaqzT4ugdNLcjH1XkB1WlUwYuVQJ7g4ccZuMxw130_assertion SIO_000772 17316906 NP691139.RA_Ug6NFaqzT4ugdNLcjH1XkB1WlUwYuVQJ7g4ccZuMxw130_provenance.
- NP691139.RA_Ug6NFaqzT4ugdNLcjH1XkB1WlUwYuVQJ7g4ccZuMxw130_assertion wasDerivedFrom befree-20140225 NP691139.RA_Ug6NFaqzT4ugdNLcjH1XkB1WlUwYuVQJ7g4ccZuMxw130_provenance.
- NP691139.RA_Ug6NFaqzT4ugdNLcjH1XkB1WlUwYuVQJ7g4ccZuMxw130_assertion wasGeneratedBy ECO_0000203 NP691139.RA_Ug6NFaqzT4ugdNLcjH1XkB1WlUwYuVQJ7g4ccZuMxw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP691139.RA_Ug6NFaqzT4ugdNLcjH1XkB1WlUwYuVQJ7g4ccZuMxw130_provenance.