Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP765704.RAsThaVvM_aweb13RXk2Ckn8fZpgxw65xQD8B6adOqvCY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP765704.RAsThaVvM_aweb13RXk2Ckn8fZpgxw65xQD8B6adOqvCY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP765704.RAsThaVvM_aweb13RXk2Ckn8fZpgxw65xQD8B6adOqvCY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP765704.RAsThaVvM_aweb13RXk2Ckn8fZpgxw65xQD8B6adOqvCY130_provenance.
- befree-2016 importedOn "2016-02-19" NP765704.RAsThaVvM_aweb13RXk2Ckn8fZpgxw65xQD8B6adOqvCY130_provenance.
- NP765704.RAsThaVvM_aweb13RXk2Ckn8fZpgxw65xQD8B6adOqvCY130_assertion wasGeneratedBy ECO_0000203 NP765704.RAsThaVvM_aweb13RXk2Ckn8fZpgxw65xQD8B6adOqvCY130_provenance.
- NP765704.RAsThaVvM_aweb13RXk2Ckn8fZpgxw65xQD8B6adOqvCY130_assertion wasDerivedFrom befree-2016 NP765704.RAsThaVvM_aweb13RXk2Ckn8fZpgxw65xQD8B6adOqvCY130_provenance.
- NP765704.RAsThaVvM_aweb13RXk2Ckn8fZpgxw65xQD8B6adOqvCY130_assertion SIO_000772 19785597 NP765704.RAsThaVvM_aweb13RXk2Ckn8fZpgxw65xQD8B6adOqvCY130_provenance.
- NP765704.RAsThaVvM_aweb13RXk2Ckn8fZpgxw65xQD8B6adOqvCY130_assertion evidence source_evidence_literature NP765704.RAsThaVvM_aweb13RXk2Ckn8fZpgxw65xQD8B6adOqvCY130_provenance.
- NP765704.RAsThaVvM_aweb13RXk2Ckn8fZpgxw65xQD8B6adOqvCY130_assertion description "[This observation suggests that coinheritance of mutations in KRT16 and FLG may aggravate the PC phenotype and that FLG could serve as a genetic modifier in PC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765704.RAsThaVvM_aweb13RXk2Ckn8fZpgxw65xQD8B6adOqvCY130_provenance.