Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP497220.RAHN12h-bDZLXSjZrC0ERlKkTF_1QVl8eJqJ7jHeZmeSY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP497220.RAHN12h-bDZLXSjZrC0ERlKkTF_1QVl8eJqJ7jHeZmeSY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP497220.RAHN12h-bDZLXSjZrC0ERlKkTF_1QVl8eJqJ7jHeZmeSY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP497220.RAHN12h-bDZLXSjZrC0ERlKkTF_1QVl8eJqJ7jHeZmeSY130_provenance.
- NP497220.RAHN12h-bDZLXSjZrC0ERlKkTF_1QVl8eJqJ7jHeZmeSY130_assertion description "[We have now screened 129 individuals with CPHD and isolated GH deficiency for mutations within POU1F1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP497220.RAHN12h-bDZLXSjZrC0ERlKkTF_1QVl8eJqJ7jHeZmeSY130_provenance.
- NP497220.RAHN12h-bDZLXSjZrC0ERlKkTF_1QVl8eJqJ7jHeZmeSY130_assertion evidence source_evidence_literature NP497220.RAHN12h-bDZLXSjZrC0ERlKkTF_1QVl8eJqJ7jHeZmeSY130_provenance.
- NP497220.RAHN12h-bDZLXSjZrC0ERlKkTF_1QVl8eJqJ7jHeZmeSY130_assertion SIO_000772 15928241 NP497220.RAHN12h-bDZLXSjZrC0ERlKkTF_1QVl8eJqJ7jHeZmeSY130_provenance.
- NP497220.RAHN12h-bDZLXSjZrC0ERlKkTF_1QVl8eJqJ7jHeZmeSY130_assertion wasDerivedFrom befree-2016 NP497220.RAHN12h-bDZLXSjZrC0ERlKkTF_1QVl8eJqJ7jHeZmeSY130_provenance.
- NP497220.RAHN12h-bDZLXSjZrC0ERlKkTF_1QVl8eJqJ7jHeZmeSY130_assertion wasGeneratedBy ECO_0000203 NP497220.RAHN12h-bDZLXSjZrC0ERlKkTF_1QVl8eJqJ7jHeZmeSY130_provenance.
- befree-2016 importedOn "2016-02-19" NP497220.RAHN12h-bDZLXSjZrC0ERlKkTF_1QVl8eJqJ7jHeZmeSY130_provenance.