Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1260936.RA0WaZeRL-p3Fgz28_NPHFGAwvXnrIH_30DQKH7_BsRk0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1260936.RA0WaZeRL-p3Fgz28_NPHFGAwvXnrIH_30DQKH7_BsRk0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1260936.RA0WaZeRL-p3Fgz28_NPHFGAwvXnrIH_30DQKH7_BsRk0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1260936.RA0WaZeRL-p3Fgz28_NPHFGAwvXnrIH_30DQKH7_BsRk0130_provenance.
- NP1260936.RA0WaZeRL-p3Fgz28_NPHFGAwvXnrIH_30DQKH7_BsRk0130_assertion description "[We report the phenotypes of the HLA and complement C4 and Bf genes, which are closely linked to the CYP21B gene, together with a detailed analysis of the CYP21 and C4 RFLP, in 17 Finnish families with CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260936.RA0WaZeRL-p3Fgz28_NPHFGAwvXnrIH_30DQKH7_BsRk0130_provenance.
- NP1260936.RA0WaZeRL-p3Fgz28_NPHFGAwvXnrIH_30DQKH7_BsRk0130_assertion evidence source_evidence_literature NP1260936.RA0WaZeRL-p3Fgz28_NPHFGAwvXnrIH_30DQKH7_BsRk0130_provenance.
- NP1260936.RA0WaZeRL-p3Fgz28_NPHFGAwvXnrIH_30DQKH7_BsRk0130_assertion SIO_000772 2565078 NP1260936.RA0WaZeRL-p3Fgz28_NPHFGAwvXnrIH_30DQKH7_BsRk0130_provenance.
- NP1260936.RA0WaZeRL-p3Fgz28_NPHFGAwvXnrIH_30DQKH7_BsRk0130_assertion wasDerivedFrom befree-2016 NP1260936.RA0WaZeRL-p3Fgz28_NPHFGAwvXnrIH_30DQKH7_BsRk0130_provenance.
- NP1260936.RA0WaZeRL-p3Fgz28_NPHFGAwvXnrIH_30DQKH7_BsRk0130_assertion wasGeneratedBy ECO_0000203 NP1260936.RA0WaZeRL-p3Fgz28_NPHFGAwvXnrIH_30DQKH7_BsRk0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1260936.RA0WaZeRL-p3Fgz28_NPHFGAwvXnrIH_30DQKH7_BsRk0130_provenance.