Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_assertion> ?p ?o ?g. }
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- NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_assertion type Assertion NP378872.RAD_bkGonB4b854kM2bygHl_cUZw6FJGJPCv_VdCtbwGI130_head.
- 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.