Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP939244.RAHvLRJLT4F30zZ1gmlPzed4N42GC66XJzNbE9lWaPWEI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP939244.RAHvLRJLT4F30zZ1gmlPzed4N42GC66XJzNbE9lWaPWEI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP939244.RAHvLRJLT4F30zZ1gmlPzed4N42GC66XJzNbE9lWaPWEI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP939244.RAHvLRJLT4F30zZ1gmlPzed4N42GC66XJzNbE9lWaPWEI130_provenance.
- NP939244.RAHvLRJLT4F30zZ1gmlPzed4N42GC66XJzNbE9lWaPWEI130_assertion description "[Three human diseases cosegregate with microsatellite markers used in construction of the human BAC/YAC physical map, including autosomal dominant nocturnal frontal lobe epilepsy (ENFL2; also known as ADNFLE), a syndrome of mental retardation, spasticity, and tapetoretinal degeneration (MRST); and a pyogenic arthritis, pyoderma gangrenosum, and acne syndrome (PAPA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939244.RAHvLRJLT4F30zZ1gmlPzed4N42GC66XJzNbE9lWaPWEI130_provenance.
- NP939244.RAHvLRJLT4F30zZ1gmlPzed4N42GC66XJzNbE9lWaPWEI130_assertion evidence source_evidence_literature NP939244.RAHvLRJLT4F30zZ1gmlPzed4N42GC66XJzNbE9lWaPWEI130_provenance.
- NP939244.RAHvLRJLT4F30zZ1gmlPzed4N42GC66XJzNbE9lWaPWEI130_assertion SIO_000772 11247670 NP939244.RAHvLRJLT4F30zZ1gmlPzed4N42GC66XJzNbE9lWaPWEI130_provenance.
- NP939244.RAHvLRJLT4F30zZ1gmlPzed4N42GC66XJzNbE9lWaPWEI130_assertion wasDerivedFrom befree-20140225 NP939244.RAHvLRJLT4F30zZ1gmlPzed4N42GC66XJzNbE9lWaPWEI130_provenance.
- NP939244.RAHvLRJLT4F30zZ1gmlPzed4N42GC66XJzNbE9lWaPWEI130_assertion wasGeneratedBy ECO_0000203 NP939244.RAHvLRJLT4F30zZ1gmlPzed4N42GC66XJzNbE9lWaPWEI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP939244.RAHvLRJLT4F30zZ1gmlPzed4N42GC66XJzNbE9lWaPWEI130_provenance.