Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP61498.RA1cv84rZMJWV7osvHYm906zy-dgkEFRwR-CUhoGU9Nqw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP61498.RA1cv84rZMJWV7osvHYm906zy-dgkEFRwR-CUhoGU9Nqw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP61498.RA1cv84rZMJWV7osvHYm906zy-dgkEFRwR-CUhoGU9Nqw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP61498.RA1cv84rZMJWV7osvHYm906zy-dgkEFRwR-CUhoGU9Nqw130_provenance.
- NP61498.RA1cv84rZMJWV7osvHYm906zy-dgkEFRwR-CUhoGU9Nqw130_assertion description "[Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP61498.RA1cv84rZMJWV7osvHYm906zy-dgkEFRwR-CUhoGU9Nqw130_provenance.
- NP61498.RA1cv84rZMJWV7osvHYm906zy-dgkEFRwR-CUhoGU9Nqw130_assertion evidence source_evidence_literature NP61498.RA1cv84rZMJWV7osvHYm906zy-dgkEFRwR-CUhoGU9Nqw130_provenance.
- NP61498.RA1cv84rZMJWV7osvHYm906zy-dgkEFRwR-CUhoGU9Nqw130_assertion SIO_000772 15017103 NP61498.RA1cv84rZMJWV7osvHYm906zy-dgkEFRwR-CUhoGU9Nqw130_provenance.
- NP61498.RA1cv84rZMJWV7osvHYm906zy-dgkEFRwR-CUhoGU9Nqw130_assertion wasDerivedFrom gad-20150221 NP61498.RA1cv84rZMJWV7osvHYm906zy-dgkEFRwR-CUhoGU9Nqw130_provenance.
- NP61498.RA1cv84rZMJWV7osvHYm906zy-dgkEFRwR-CUhoGU9Nqw130_assertion wasGeneratedBy ECO_0000203 NP61498.RA1cv84rZMJWV7osvHYm906zy-dgkEFRwR-CUhoGU9Nqw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP61498.RA1cv84rZMJWV7osvHYm906zy-dgkEFRwR-CUhoGU9Nqw130_provenance.