Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP694222.RALHyO4gZPHWSJRzA6XidIQvT9Q_v5xxdiNCn2Z_BcmB0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP694222.RALHyO4gZPHWSJRzA6XidIQvT9Q_v5xxdiNCn2Z_BcmB0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694222.RALHyO4gZPHWSJRzA6XidIQvT9Q_v5xxdiNCn2Z_BcmB0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694222.RALHyO4gZPHWSJRzA6XidIQvT9Q_v5xxdiNCn2Z_BcmB0130_provenance.
- NP694222.RALHyO4gZPHWSJRzA6XidIQvT9Q_v5xxdiNCn2Z_BcmB0130_assertion description "[Oculopharyngeal muscular dystrophy (OPMD) is an adult-onset disease caused by expanded (GCN)12-17 stretches encoding the N-terminal polyalanine domain of the poly(A) binding protein nuclear 1 (PABPN1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694222.RALHyO4gZPHWSJRzA6XidIQvT9Q_v5xxdiNCn2Z_BcmB0130_provenance.
- NP694222.RALHyO4gZPHWSJRzA6XidIQvT9Q_v5xxdiNCn2Z_BcmB0130_assertion evidence source_evidence_literature NP694222.RALHyO4gZPHWSJRzA6XidIQvT9Q_v5xxdiNCn2Z_BcmB0130_provenance.
- NP694222.RALHyO4gZPHWSJRzA6XidIQvT9Q_v5xxdiNCn2Z_BcmB0130_assertion SIO_000772 15755682 NP694222.RALHyO4gZPHWSJRzA6XidIQvT9Q_v5xxdiNCn2Z_BcmB0130_provenance.
- NP694222.RALHyO4gZPHWSJRzA6XidIQvT9Q_v5xxdiNCn2Z_BcmB0130_assertion wasDerivedFrom befree-20140225 NP694222.RALHyO4gZPHWSJRzA6XidIQvT9Q_v5xxdiNCn2Z_BcmB0130_provenance.
- NP694222.RALHyO4gZPHWSJRzA6XidIQvT9Q_v5xxdiNCn2Z_BcmB0130_assertion wasGeneratedBy ECO_0000203 NP694222.RALHyO4gZPHWSJRzA6XidIQvT9Q_v5xxdiNCn2Z_BcmB0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP694222.RALHyO4gZPHWSJRzA6XidIQvT9Q_v5xxdiNCn2Z_BcmB0130_provenance.