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- source_evidence_literature type ECO_0000212 NP889510.RApZnt6tX2LxCtMqUUfgiD3GhPC6eJcz-Nor5leLz1bpA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889510.RApZnt6tX2LxCtMqUUfgiD3GhPC6eJcz-Nor5leLz1bpA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889510.RApZnt6tX2LxCtMqUUfgiD3GhPC6eJcz-Nor5leLz1bpA130_provenance.
- NP889510.RApZnt6tX2LxCtMqUUfgiD3GhPC6eJcz-Nor5leLz1bpA130_assertion description "[Identification of a novel mutation in the ANGPTL3 gene in two families diagnosed of familial hypobetalipoproteinemia without APOB mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889510.RApZnt6tX2LxCtMqUUfgiD3GhPC6eJcz-Nor5leLz1bpA130_provenance.
- NP889510.RApZnt6tX2LxCtMqUUfgiD3GhPC6eJcz-Nor5leLz1bpA130_assertion evidence source_evidence_literature NP889510.RApZnt6tX2LxCtMqUUfgiD3GhPC6eJcz-Nor5leLz1bpA130_provenance.
- NP889510.RApZnt6tX2LxCtMqUUfgiD3GhPC6eJcz-Nor5leLz1bpA130_assertion SIO_000772 22155345 NP889510.RApZnt6tX2LxCtMqUUfgiD3GhPC6eJcz-Nor5leLz1bpA130_provenance.
- NP889510.RApZnt6tX2LxCtMqUUfgiD3GhPC6eJcz-Nor5leLz1bpA130_assertion wasDerivedFrom befree-20150227 NP889510.RApZnt6tX2LxCtMqUUfgiD3GhPC6eJcz-Nor5leLz1bpA130_provenance.
- NP889510.RApZnt6tX2LxCtMqUUfgiD3GhPC6eJcz-Nor5leLz1bpA130_assertion wasGeneratedBy ECO_0000203 NP889510.RApZnt6tX2LxCtMqUUfgiD3GhPC6eJcz-Nor5leLz1bpA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP889510.RApZnt6tX2LxCtMqUUfgiD3GhPC6eJcz-Nor5leLz1bpA130_provenance.