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- source_evidence_literature type ECO_0000212 NP95267.RAWQbxfkU-c7CAGJeQlmsNJmaJHY4nybnYMJ9pO2UHh5E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP95267.RAWQbxfkU-c7CAGJeQlmsNJmaJHY4nybnYMJ9pO2UHh5E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP95267.RAWQbxfkU-c7CAGJeQlmsNJmaJHY4nybnYMJ9pO2UHh5E130_provenance.
- NP95267.RAWQbxfkU-c7CAGJeQlmsNJmaJHY4nybnYMJ9pO2UHh5E130_assertion description "[ Although more detailed functional characterizations of these polymorphisms remain to be undertaken, these polymorphic sites may be useful for identifying alleles associated with mis-splicing, additional transcript factors and, more generally, in cancer-s]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95267.RAWQbxfkU-c7CAGJeQlmsNJmaJHY4nybnYMJ9pO2UHh5E130_provenance.
- NP95267.RAWQbxfkU-c7CAGJeQlmsNJmaJHY4nybnYMJ9pO2UHh5E130_assertion evidence source_evidence_literature NP95267.RAWQbxfkU-c7CAGJeQlmsNJmaJHY4nybnYMJ9pO2UHh5E130_provenance.
- NP95267.RAWQbxfkU-c7CAGJeQlmsNJmaJHY4nybnYMJ9pO2UHh5E130_assertion SIO_000772 16127747 NP95267.RAWQbxfkU-c7CAGJeQlmsNJmaJHY4nybnYMJ9pO2UHh5E130_provenance.
- NP95267.RAWQbxfkU-c7CAGJeQlmsNJmaJHY4nybnYMJ9pO2UHh5E130_assertion wasDerivedFrom gad-20150221 NP95267.RAWQbxfkU-c7CAGJeQlmsNJmaJHY4nybnYMJ9pO2UHh5E130_provenance.
- NP95267.RAWQbxfkU-c7CAGJeQlmsNJmaJHY4nybnYMJ9pO2UHh5E130_assertion wasGeneratedBy ECO_0000203 NP95267.RAWQbxfkU-c7CAGJeQlmsNJmaJHY4nybnYMJ9pO2UHh5E130_provenance.
- gad-20150221 importedOn "2015-02-21" NP95267.RAWQbxfkU-c7CAGJeQlmsNJmaJHY4nybnYMJ9pO2UHh5E130_provenance.