Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_provenance.
- NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_assertion description "[These results demonstrate that the ATXN2 CAG expansion is the sole causative mutation responsible for SCA2-P, and that genetic modifiers may not be the major cause of the phenotypic diversity of SCA2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_provenance.
- NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_assertion evidence source_evidence_literature NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_provenance.
- NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_assertion SIO_000772 25189117 NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_provenance.
- NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_assertion wasDerivedFrom befree-2016 NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_provenance.
- NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_assertion wasGeneratedBy ECO_0000203 NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_provenance.