Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP694221.RADP9mc63tOE-SYseZKbOz31vvgpfNKVIX-0LuEn2aErA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP694221.RADP9mc63tOE-SYseZKbOz31vvgpfNKVIX-0LuEn2aErA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694221.RADP9mc63tOE-SYseZKbOz31vvgpfNKVIX-0LuEn2aErA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694221.RADP9mc63tOE-SYseZKbOz31vvgpfNKVIX-0LuEn2aErA130_provenance.
- NP694221.RADP9mc63tOE-SYseZKbOz31vvgpfNKVIX-0LuEn2aErA130_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." NP694221.RADP9mc63tOE-SYseZKbOz31vvgpfNKVIX-0LuEn2aErA130_provenance.
- NP694221.RADP9mc63tOE-SYseZKbOz31vvgpfNKVIX-0LuEn2aErA130_assertion evidence source_evidence_literature NP694221.RADP9mc63tOE-SYseZKbOz31vvgpfNKVIX-0LuEn2aErA130_provenance.
- NP694221.RADP9mc63tOE-SYseZKbOz31vvgpfNKVIX-0LuEn2aErA130_assertion SIO_000772 18805914 NP694221.RADP9mc63tOE-SYseZKbOz31vvgpfNKVIX-0LuEn2aErA130_provenance.
- NP694221.RADP9mc63tOE-SYseZKbOz31vvgpfNKVIX-0LuEn2aErA130_assertion wasDerivedFrom befree-2016 NP694221.RADP9mc63tOE-SYseZKbOz31vvgpfNKVIX-0LuEn2aErA130_provenance.
- NP694221.RADP9mc63tOE-SYseZKbOz31vvgpfNKVIX-0LuEn2aErA130_assertion wasGeneratedBy ECO_0000203 NP694221.RADP9mc63tOE-SYseZKbOz31vvgpfNKVIX-0LuEn2aErA130_provenance.
- befree-2016 importedOn "2016-02-19" NP694221.RADP9mc63tOE-SYseZKbOz31vvgpfNKVIX-0LuEn2aErA130_provenance.