Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP575256.RARmmOx9rFccAIh9T6KQ5gnZCHUcwkzog9cG6inBLu8fw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP575256.RARmmOx9rFccAIh9T6KQ5gnZCHUcwkzog9cG6inBLu8fw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP575256.RARmmOx9rFccAIh9T6KQ5gnZCHUcwkzog9cG6inBLu8fw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP575256.RARmmOx9rFccAIh9T6KQ5gnZCHUcwkzog9cG6inBLu8fw130_provenance.
- NP575256.RARmmOx9rFccAIh9T6KQ5gnZCHUcwkzog9cG6inBLu8fw130_assertion description "[AGS (MIM 225750) is a genetically-determined encephalopathy characterized by severe neurological dysfunction, acquired microcephaly associated with severe prognosis quoad valetudinem, and less frequently also quoad vitam.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575256.RARmmOx9rFccAIh9T6KQ5gnZCHUcwkzog9cG6inBLu8fw130_provenance.
- NP575256.RARmmOx9rFccAIh9T6KQ5gnZCHUcwkzog9cG6inBLu8fw130_assertion evidence source_evidence_literature NP575256.RARmmOx9rFccAIh9T6KQ5gnZCHUcwkzog9cG6inBLu8fw130_provenance.
- NP575256.RARmmOx9rFccAIh9T6KQ5gnZCHUcwkzog9cG6inBLu8fw130_assertion SIO_000772 22940555 NP575256.RARmmOx9rFccAIh9T6KQ5gnZCHUcwkzog9cG6inBLu8fw130_provenance.
- NP575256.RARmmOx9rFccAIh9T6KQ5gnZCHUcwkzog9cG6inBLu8fw130_assertion wasDerivedFrom befree-20140225 NP575256.RARmmOx9rFccAIh9T6KQ5gnZCHUcwkzog9cG6inBLu8fw130_provenance.
- NP575256.RARmmOx9rFccAIh9T6KQ5gnZCHUcwkzog9cG6inBLu8fw130_assertion wasGeneratedBy ECO_0000203 NP575256.RARmmOx9rFccAIh9T6KQ5gnZCHUcwkzog9cG6inBLu8fw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP575256.RARmmOx9rFccAIh9T6KQ5gnZCHUcwkzog9cG6inBLu8fw130_provenance.