Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP164155.RACshlKykeKDo3uthbvVo5jMOLpKjI6fmzf3aBeXg8WaA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP164155.RACshlKykeKDo3uthbvVo5jMOLpKjI6fmzf3aBeXg8WaA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP164155.RACshlKykeKDo3uthbvVo5jMOLpKjI6fmzf3aBeXg8WaA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP164155.RACshlKykeKDo3uthbvVo5jMOLpKjI6fmzf3aBeXg8WaA130_provenance.
- NP164155.RACshlKykeKDo3uthbvVo5jMOLpKjI6fmzf3aBeXg8WaA130_assertion description "[In addition, these findings are compatible with a modifying role for the centromeric SMN genes and the NAIP genes in the severity of the SMA phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164155.RACshlKykeKDo3uthbvVo5jMOLpKjI6fmzf3aBeXg8WaA130_provenance.
- NP164155.RACshlKykeKDo3uthbvVo5jMOLpKjI6fmzf3aBeXg8WaA130_assertion evidence source_evidence_literature NP164155.RACshlKykeKDo3uthbvVo5jMOLpKjI6fmzf3aBeXg8WaA130_provenance.
- NP164155.RACshlKykeKDo3uthbvVo5jMOLpKjI6fmzf3aBeXg8WaA130_assertion SIO_000772 8957014 NP164155.RACshlKykeKDo3uthbvVo5jMOLpKjI6fmzf3aBeXg8WaA130_provenance.
- NP164155.RACshlKykeKDo3uthbvVo5jMOLpKjI6fmzf3aBeXg8WaA130_assertion wasDerivedFrom befree-20140225 NP164155.RACshlKykeKDo3uthbvVo5jMOLpKjI6fmzf3aBeXg8WaA130_provenance.
- NP164155.RACshlKykeKDo3uthbvVo5jMOLpKjI6fmzf3aBeXg8WaA130_assertion wasGeneratedBy ECO_0000203 NP164155.RACshlKykeKDo3uthbvVo5jMOLpKjI6fmzf3aBeXg8WaA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP164155.RACshlKykeKDo3uthbvVo5jMOLpKjI6fmzf3aBeXg8WaA130_provenance.