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- source_evidence_literature type ECO_0000212 NP674521.RAaXgjL-XgqpYE70AY2dZU9FH-MRHhT7oyrBQ8gOzp7a8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674521.RAaXgjL-XgqpYE70AY2dZU9FH-MRHhT7oyrBQ8gOzp7a8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674521.RAaXgjL-XgqpYE70AY2dZU9FH-MRHhT7oyrBQ8gOzp7a8130_provenance.
- NP674521.RAaXgjL-XgqpYE70AY2dZU9FH-MRHhT7oyrBQ8gOzp7a8130_assertion description "[In another XLRP family, a nonsense mutation (g.ORF15+810G>T) was identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674521.RAaXgjL-XgqpYE70AY2dZU9FH-MRHhT7oyrBQ8gOzp7a8130_provenance.
- NP674521.RAaXgjL-XgqpYE70AY2dZU9FH-MRHhT7oyrBQ8gOzp7a8130_assertion evidence source_evidence_literature NP674521.RAaXgjL-XgqpYE70AY2dZU9FH-MRHhT7oyrBQ8gOzp7a8130_provenance.
- NP674521.RAaXgjL-XgqpYE70AY2dZU9FH-MRHhT7oyrBQ8gOzp7a8130_assertion SIO_000772 21683121 NP674521.RAaXgjL-XgqpYE70AY2dZU9FH-MRHhT7oyrBQ8gOzp7a8130_provenance.
- NP674521.RAaXgjL-XgqpYE70AY2dZU9FH-MRHhT7oyrBQ8gOzp7a8130_assertion wasDerivedFrom befree-20150227 NP674521.RAaXgjL-XgqpYE70AY2dZU9FH-MRHhT7oyrBQ8gOzp7a8130_provenance.
- NP674521.RAaXgjL-XgqpYE70AY2dZU9FH-MRHhT7oyrBQ8gOzp7a8130_assertion wasGeneratedBy ECO_0000203 NP674521.RAaXgjL-XgqpYE70AY2dZU9FH-MRHhT7oyrBQ8gOzp7a8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674521.RAaXgjL-XgqpYE70AY2dZU9FH-MRHhT7oyrBQ8gOzp7a8130_provenance.