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- source_evidence_literature type ECO_0000212 NP923894.RAtI1ImPimfjhn_0a9iX-X0nP4JtnnvhM0X0RBJn6sN70130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP923894.RAtI1ImPimfjhn_0a9iX-X0nP4JtnnvhM0X0RBJn6sN70130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP923894.RAtI1ImPimfjhn_0a9iX-X0nP4JtnnvhM0X0RBJn6sN70130_provenance.
- befree-2016 importedOn "2016-02-19" NP923894.RAtI1ImPimfjhn_0a9iX-X0nP4JtnnvhM0X0RBJn6sN70130_provenance.
- NP923894.RAtI1ImPimfjhn_0a9iX-X0nP4JtnnvhM0X0RBJn6sN70130_assertion wasGeneratedBy ECO_0000203 NP923894.RAtI1ImPimfjhn_0a9iX-X0nP4JtnnvhM0X0RBJn6sN70130_provenance.
- NP923894.RAtI1ImPimfjhn_0a9iX-X0nP4JtnnvhM0X0RBJn6sN70130_assertion wasDerivedFrom befree-2016 NP923894.RAtI1ImPimfjhn_0a9iX-X0nP4JtnnvhM0X0RBJn6sN70130_provenance.
- NP923894.RAtI1ImPimfjhn_0a9iX-X0nP4JtnnvhM0X0RBJn6sN70130_assertion SIO_000772 21917868 NP923894.RAtI1ImPimfjhn_0a9iX-X0nP4JtnnvhM0X0RBJn6sN70130_provenance.
- NP923894.RAtI1ImPimfjhn_0a9iX-X0nP4JtnnvhM0X0RBJn6sN70130_assertion evidence source_evidence_literature NP923894.RAtI1ImPimfjhn_0a9iX-X0nP4JtnnvhM0X0RBJn6sN70130_provenance.
- NP923894.RAtI1ImPimfjhn_0a9iX-X0nP4JtnnvhM0X0RBJn6sN70130_assertion description "[Multiple endocrine neoplasia type 1 (MEN1) is caused by mutations in the menin (MEN1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP923894.RAtI1ImPimfjhn_0a9iX-X0nP4JtnnvhM0X0RBJn6sN70130_provenance.