Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246161.RAKLm3hBXKV2YzI1kKicJCrstYDV8qGMDR7-JwkGfddvE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1246161.RAKLm3hBXKV2YzI1kKicJCrstYDV8qGMDR7-JwkGfddvE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246161.RAKLm3hBXKV2YzI1kKicJCrstYDV8qGMDR7-JwkGfddvE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246161.RAKLm3hBXKV2YzI1kKicJCrstYDV8qGMDR7-JwkGfddvE130_provenance.
- NP1246161.RAKLm3hBXKV2YzI1kKicJCrstYDV8qGMDR7-JwkGfddvE130_assertion description "[Familial cardiofaciocutaneous syndrome in a father and a son with a novel MEK2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246161.RAKLm3hBXKV2YzI1kKicJCrstYDV8qGMDR7-JwkGfddvE130_provenance.
- NP1246161.RAKLm3hBXKV2YzI1kKicJCrstYDV8qGMDR7-JwkGfddvE130_assertion evidence source_evidence_literature NP1246161.RAKLm3hBXKV2YzI1kKicJCrstYDV8qGMDR7-JwkGfddvE130_provenance.
- NP1246161.RAKLm3hBXKV2YzI1kKicJCrstYDV8qGMDR7-JwkGfddvE130_assertion SIO_000772 25487361 NP1246161.RAKLm3hBXKV2YzI1kKicJCrstYDV8qGMDR7-JwkGfddvE130_provenance.
- NP1246161.RAKLm3hBXKV2YzI1kKicJCrstYDV8qGMDR7-JwkGfddvE130_assertion wasDerivedFrom befree-2016 NP1246161.RAKLm3hBXKV2YzI1kKicJCrstYDV8qGMDR7-JwkGfddvE130_provenance.
- NP1246161.RAKLm3hBXKV2YzI1kKicJCrstYDV8qGMDR7-JwkGfddvE130_assertion wasGeneratedBy ECO_0000203 NP1246161.RAKLm3hBXKV2YzI1kKicJCrstYDV8qGMDR7-JwkGfddvE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246161.RAKLm3hBXKV2YzI1kKicJCrstYDV8qGMDR7-JwkGfddvE130_provenance.