Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP151939.RANDU0_nxG_wq7D6VK2hDTbfVrOZJ0OviaJXuGJACrBuk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP151939.RANDU0_nxG_wq7D6VK2hDTbfVrOZJ0OviaJXuGJACrBuk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP151939.RANDU0_nxG_wq7D6VK2hDTbfVrOZJ0OviaJXuGJACrBuk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP151939.RANDU0_nxG_wq7D6VK2hDTbfVrOZJ0OviaJXuGJACrBuk130_provenance.
- NP151939.RANDU0_nxG_wq7D6VK2hDTbfVrOZJ0OviaJXuGJACrBuk130_assertion wasGeneratedBy ECO_0000203 NP151939.RANDU0_nxG_wq7D6VK2hDTbfVrOZJ0OviaJXuGJACrBuk130_provenance.
- NP151939.RANDU0_nxG_wq7D6VK2hDTbfVrOZJ0OviaJXuGJACrBuk130_assertion wasDerivedFrom lhgdn-20090331 NP151939.RANDU0_nxG_wq7D6VK2hDTbfVrOZJ0OviaJXuGJACrBuk130_provenance.
- NP151939.RANDU0_nxG_wq7D6VK2hDTbfVrOZJ0OviaJXuGJACrBuk130_assertion SIO_000772 18580586 NP151939.RANDU0_nxG_wq7D6VK2hDTbfVrOZJ0OviaJXuGJACrBuk130_provenance.
- NP151939.RANDU0_nxG_wq7D6VK2hDTbfVrOZJ0OviaJXuGJACrBuk130_assertion evidence source_evidence_literature NP151939.RANDU0_nxG_wq7D6VK2hDTbfVrOZJ0OviaJXuGJACrBuk130_provenance.
- NP151939.RANDU0_nxG_wq7D6VK2hDTbfVrOZJ0OviaJXuGJACrBuk130_assertion description "[first description of neuropathologic findings in early onset familial Alzheimer disease (EOFAD) due to N135S PSEN1 mutation; clinical phenotype was remarkable for spastic dysarthria, limb spasticity & seizures, in addition to more typical features of EOFAD ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151939.RANDU0_nxG_wq7D6VK2hDTbfVrOZJ0OviaJXuGJACrBuk130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP151939.RANDU0_nxG_wq7D6VK2hDTbfVrOZJ0OviaJXuGJACrBuk130_provenance.