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- source_evidence_literature type ECO_0000212 NP668531.RAMrbbqjDie9NYmMux41mU8tfSwiXfhYJDQPjGyBhxhes130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668531.RAMrbbqjDie9NYmMux41mU8tfSwiXfhYJDQPjGyBhxhes130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668531.RAMrbbqjDie9NYmMux41mU8tfSwiXfhYJDQPjGyBhxhes130_provenance.
- NP668531.RAMrbbqjDie9NYmMux41mU8tfSwiXfhYJDQPjGyBhxhes130_assertion description "[The authors identified a novel peripherin/RDS gene mutation associated with autosomal dominant retinal degeneration in patients from three different families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668531.RAMrbbqjDie9NYmMux41mU8tfSwiXfhYJDQPjGyBhxhes130_provenance.
- NP668531.RAMrbbqjDie9NYmMux41mU8tfSwiXfhYJDQPjGyBhxhes130_assertion evidence source_evidence_literature NP668531.RAMrbbqjDie9NYmMux41mU8tfSwiXfhYJDQPjGyBhxhes130_provenance.
- NP668531.RAMrbbqjDie9NYmMux41mU8tfSwiXfhYJDQPjGyBhxhes130_assertion SIO_000772 7862413 NP668531.RAMrbbqjDie9NYmMux41mU8tfSwiXfhYJDQPjGyBhxhes130_provenance.
- NP668531.RAMrbbqjDie9NYmMux41mU8tfSwiXfhYJDQPjGyBhxhes130_assertion wasDerivedFrom befree-20150227 NP668531.RAMrbbqjDie9NYmMux41mU8tfSwiXfhYJDQPjGyBhxhes130_provenance.
- NP668531.RAMrbbqjDie9NYmMux41mU8tfSwiXfhYJDQPjGyBhxhes130_assertion wasGeneratedBy ECO_0000203 NP668531.RAMrbbqjDie9NYmMux41mU8tfSwiXfhYJDQPjGyBhxhes130_provenance.
- befree-20150227 importedOn "2015-02-27" NP668531.RAMrbbqjDie9NYmMux41mU8tfSwiXfhYJDQPjGyBhxhes130_provenance.