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- source_evidence_literature type ECO_0000212 NP211452.RAiJYAwRmNfNA0VLk0yMnhHkgYb9XGNv_Vpb4roV05Ot4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP211452.RAiJYAwRmNfNA0VLk0yMnhHkgYb9XGNv_Vpb4roV05Ot4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP211452.RAiJYAwRmNfNA0VLk0yMnhHkgYb9XGNv_Vpb4roV05Ot4130_provenance.
- NP211452.RAiJYAwRmNfNA0VLk0yMnhHkgYb9XGNv_Vpb4roV05Ot4130_assertion description "[Substantial discrimination between predicted functional classes of RET mutations and disease severity even for a multigenic disease such as Hirschsprung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211452.RAiJYAwRmNfNA0VLk0yMnhHkgYb9XGNv_Vpb4roV05Ot4130_provenance.
- NP211452.RAiJYAwRmNfNA0VLk0yMnhHkgYb9XGNv_Vpb4roV05Ot4130_assertion evidence source_evidence_literature NP211452.RAiJYAwRmNfNA0VLk0yMnhHkgYb9XGNv_Vpb4roV05Ot4130_provenance.
- NP211452.RAiJYAwRmNfNA0VLk0yMnhHkgYb9XGNv_Vpb4roV05Ot4130_assertion SIO_000772 15956201 NP211452.RAiJYAwRmNfNA0VLk0yMnhHkgYb9XGNv_Vpb4roV05Ot4130_provenance.
- NP211452.RAiJYAwRmNfNA0VLk0yMnhHkgYb9XGNv_Vpb4roV05Ot4130_assertion wasDerivedFrom lhgdn-20090331 NP211452.RAiJYAwRmNfNA0VLk0yMnhHkgYb9XGNv_Vpb4roV05Ot4130_provenance.
- NP211452.RAiJYAwRmNfNA0VLk0yMnhHkgYb9XGNv_Vpb4roV05Ot4130_assertion wasGeneratedBy ECO_0000203 NP211452.RAiJYAwRmNfNA0VLk0yMnhHkgYb9XGNv_Vpb4roV05Ot4130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP211452.RAiJYAwRmNfNA0VLk0yMnhHkgYb9XGNv_Vpb4roV05Ot4130_provenance.