Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP481988.RA50t3M4UmsVmOlTvGCM2DHX6WC1ltq1Gu2ylp26Ux110130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP481988.RA50t3M4UmsVmOlTvGCM2DHX6WC1ltq1Gu2ylp26Ux110130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP481988.RA50t3M4UmsVmOlTvGCM2DHX6WC1ltq1Gu2ylp26Ux110130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP481988.RA50t3M4UmsVmOlTvGCM2DHX6WC1ltq1Gu2ylp26Ux110130_provenance.
- NP481988.RA50t3M4UmsVmOlTvGCM2DHX6WC1ltq1Gu2ylp26Ux110130_assertion description "[Clearly, low IGF1 levels are evidence of persistent severe GHD in subjects with genetic GHD or panhypopituitarism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP481988.RA50t3M4UmsVmOlTvGCM2DHX6WC1ltq1Gu2ylp26Ux110130_provenance.
- NP481988.RA50t3M4UmsVmOlTvGCM2DHX6WC1ltq1Gu2ylp26Ux110130_assertion evidence source_evidence_literature NP481988.RA50t3M4UmsVmOlTvGCM2DHX6WC1ltq1Gu2ylp26Ux110130_provenance.
- NP481988.RA50t3M4UmsVmOlTvGCM2DHX6WC1ltq1Gu2ylp26Ux110130_assertion SIO_000772 18805914 NP481988.RA50t3M4UmsVmOlTvGCM2DHX6WC1ltq1Gu2ylp26Ux110130_provenance.
- NP481988.RA50t3M4UmsVmOlTvGCM2DHX6WC1ltq1Gu2ylp26Ux110130_assertion wasDerivedFrom befree-20150227 NP481988.RA50t3M4UmsVmOlTvGCM2DHX6WC1ltq1Gu2ylp26Ux110130_provenance.
- NP481988.RA50t3M4UmsVmOlTvGCM2DHX6WC1ltq1Gu2ylp26Ux110130_assertion wasGeneratedBy ECO_0000203 NP481988.RA50t3M4UmsVmOlTvGCM2DHX6WC1ltq1Gu2ylp26Ux110130_provenance.
- befree-20150227 importedOn "2015-02-27" NP481988.RA50t3M4UmsVmOlTvGCM2DHX6WC1ltq1Gu2ylp26Ux110130_provenance.