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- source_evidence_literature type ECO_0000212 NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_provenance.
- NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_assertion description "[Using exome sequencing, we identified recurrent somatic mutations in EIF1AX and SF3B1, specifically occurring in uveal melanomas with disomy 3, which rarely metastasize.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_provenance.
- NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_assertion evidence source_evidence_literature NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_provenance.
- NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_assertion SIO_000772 23793026 NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_provenance.
- NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_assertion wasDerivedFrom befree-20150227 NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_provenance.
- NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_assertion wasGeneratedBy ECO_0000203 NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_provenance.