Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_provenance.
- befree-2016 importedOn "2016-02-19" NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_provenance.
- NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_assertion wasGeneratedBy ECO_0000203 NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_provenance.
- NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_assertion wasDerivedFrom befree-2016 NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_provenance.
- NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_assertion SIO_000772 12503101 NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_provenance.
- NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_assertion evidence source_evidence_literature NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_provenance.
- NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_assertion description "[Molecular, biochemical, and phenotypic analysis of a hemizygous male with a severe atypical phenotype for X-linked dominant Conradi-Hunermann-Happle syndrome and a mutation in EBP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_provenance.