Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP164677.RAchTkO19J_CiFnO0lqGdznn8o5AdmWIKrg2VDbmWD_GQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP164677.RAchTkO19J_CiFnO0lqGdznn8o5AdmWIKrg2VDbmWD_GQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP164677.RAchTkO19J_CiFnO0lqGdznn8o5AdmWIKrg2VDbmWD_GQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP164677.RAchTkO19J_CiFnO0lqGdznn8o5AdmWIKrg2VDbmWD_GQ130_provenance.
- NP164677.RAchTkO19J_CiFnO0lqGdznn8o5AdmWIKrg2VDbmWD_GQ130_assertion description "[We found no evidence to support the role of any common SERPING1 variants, including the rs2511989 variant, in the susceptibility to PCV in a Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164677.RAchTkO19J_CiFnO0lqGdznn8o5AdmWIKrg2VDbmWD_GQ130_provenance.
- NP164677.RAchTkO19J_CiFnO0lqGdznn8o5AdmWIKrg2VDbmWD_GQ130_assertion evidence source_evidence_literature NP164677.RAchTkO19J_CiFnO0lqGdznn8o5AdmWIKrg2VDbmWD_GQ130_provenance.
- NP164677.RAchTkO19J_CiFnO0lqGdznn8o5AdmWIKrg2VDbmWD_GQ130_assertion SIO_000772 20161815 NP164677.RAchTkO19J_CiFnO0lqGdznn8o5AdmWIKrg2VDbmWD_GQ130_provenance.
- NP164677.RAchTkO19J_CiFnO0lqGdznn8o5AdmWIKrg2VDbmWD_GQ130_assertion wasDerivedFrom gad-20150221 NP164677.RAchTkO19J_CiFnO0lqGdznn8o5AdmWIKrg2VDbmWD_GQ130_provenance.
- NP164677.RAchTkO19J_CiFnO0lqGdznn8o5AdmWIKrg2VDbmWD_GQ130_assertion wasGeneratedBy ECO_0000203 NP164677.RAchTkO19J_CiFnO0lqGdznn8o5AdmWIKrg2VDbmWD_GQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP164677.RAchTkO19J_CiFnO0lqGdznn8o5AdmWIKrg2VDbmWD_GQ130_provenance.