Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP900181.RA5NiXQ5gZ4sVwXciLlZJ-fxh7SAtECP1EhE541LF3GPQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP900181.RA5NiXQ5gZ4sVwXciLlZJ-fxh7SAtECP1EhE541LF3GPQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900181.RA5NiXQ5gZ4sVwXciLlZJ-fxh7SAtECP1EhE541LF3GPQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900181.RA5NiXQ5gZ4sVwXciLlZJ-fxh7SAtECP1EhE541LF3GPQ130_provenance.
- NP900181.RA5NiXQ5gZ4sVwXciLlZJ-fxh7SAtECP1EhE541LF3GPQ130_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." NP900181.RA5NiXQ5gZ4sVwXciLlZJ-fxh7SAtECP1EhE541LF3GPQ130_provenance.
- NP900181.RA5NiXQ5gZ4sVwXciLlZJ-fxh7SAtECP1EhE541LF3GPQ130_assertion evidence source_evidence_literature NP900181.RA5NiXQ5gZ4sVwXciLlZJ-fxh7SAtECP1EhE541LF3GPQ130_provenance.
- NP900181.RA5NiXQ5gZ4sVwXciLlZJ-fxh7SAtECP1EhE541LF3GPQ130_assertion SIO_000772 11247670 NP900181.RA5NiXQ5gZ4sVwXciLlZJ-fxh7SAtECP1EhE541LF3GPQ130_provenance.
- NP900181.RA5NiXQ5gZ4sVwXciLlZJ-fxh7SAtECP1EhE541LF3GPQ130_assertion wasDerivedFrom befree-20150227 NP900181.RA5NiXQ5gZ4sVwXciLlZJ-fxh7SAtECP1EhE541LF3GPQ130_provenance.
- NP900181.RA5NiXQ5gZ4sVwXciLlZJ-fxh7SAtECP1EhE541LF3GPQ130_assertion wasGeneratedBy ECO_0000203 NP900181.RA5NiXQ5gZ4sVwXciLlZJ-fxh7SAtECP1EhE541LF3GPQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP900181.RA5NiXQ5gZ4sVwXciLlZJ-fxh7SAtECP1EhE541LF3GPQ130_provenance.