Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP632965.RAe1LSxeardNtw4k4AtJFu7ENz6lRfSDNbzeMM2-Vg4C0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP632965.RAe1LSxeardNtw4k4AtJFu7ENz6lRfSDNbzeMM2-Vg4C0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP632965.RAe1LSxeardNtw4k4AtJFu7ENz6lRfSDNbzeMM2-Vg4C0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP632965.RAe1LSxeardNtw4k4AtJFu7ENz6lRfSDNbzeMM2-Vg4C0130_provenance.
- NP632965.RAe1LSxeardNtw4k4AtJFu7ENz6lRfSDNbzeMM2-Vg4C0130_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." NP632965.RAe1LSxeardNtw4k4AtJFu7ENz6lRfSDNbzeMM2-Vg4C0130_provenance.
- NP632965.RAe1LSxeardNtw4k4AtJFu7ENz6lRfSDNbzeMM2-Vg4C0130_assertion evidence source_evidence_literature NP632965.RAe1LSxeardNtw4k4AtJFu7ENz6lRfSDNbzeMM2-Vg4C0130_provenance.
- NP632965.RAe1LSxeardNtw4k4AtJFu7ENz6lRfSDNbzeMM2-Vg4C0130_assertion SIO_000772 11247670 NP632965.RAe1LSxeardNtw4k4AtJFu7ENz6lRfSDNbzeMM2-Vg4C0130_provenance.
- NP632965.RAe1LSxeardNtw4k4AtJFu7ENz6lRfSDNbzeMM2-Vg4C0130_assertion wasDerivedFrom befree-20140225 NP632965.RAe1LSxeardNtw4k4AtJFu7ENz6lRfSDNbzeMM2-Vg4C0130_provenance.
- NP632965.RAe1LSxeardNtw4k4AtJFu7ENz6lRfSDNbzeMM2-Vg4C0130_assertion wasGeneratedBy ECO_0000203 NP632965.RAe1LSxeardNtw4k4AtJFu7ENz6lRfSDNbzeMM2-Vg4C0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP632965.RAe1LSxeardNtw4k4AtJFu7ENz6lRfSDNbzeMM2-Vg4C0130_provenance.