Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_provenance.
- NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_assertion description "[Of the 97 amino acid substitutions, 11 occurred at a frequency that made them unlikely to be high-penetrance recessive disease-causing variants (HPRDCV). After accounting for variants in cis, one or more changes that were compatible with HPRDCV were found]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_provenance.
- NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_assertion evidence source_evidence_literature NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_provenance.
- NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_assertion SIO_000772 11328725 NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_provenance.
- NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_assertion wasDerivedFrom gad-20150221 NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_provenance.
- NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_assertion wasGeneratedBy ECO_0000203 NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_provenance.