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- source_evidence_literature type ECO_0000212 NP651266.RA4EMTAAB3qo4P6tIZGjhDPZ4poFIG3NWC-Xh0_-niB6I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651266.RA4EMTAAB3qo4P6tIZGjhDPZ4poFIG3NWC-Xh0_-niB6I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651266.RA4EMTAAB3qo4P6tIZGjhDPZ4poFIG3NWC-Xh0_-niB6I130_provenance.
- NP651266.RA4EMTAAB3qo4P6tIZGjhDPZ4poFIG3NWC-Xh0_-niB6I130_assertion description "[Intragenic polymorphisms in the retinal fascin gene provided evidence for the exclusion of this candidate as the RP17 disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651266.RA4EMTAAB3qo4P6tIZGjhDPZ4poFIG3NWC-Xh0_-niB6I130_provenance.
- NP651266.RA4EMTAAB3qo4P6tIZGjhDPZ4poFIG3NWC-Xh0_-niB6I130_assertion evidence source_evidence_literature NP651266.RA4EMTAAB3qo4P6tIZGjhDPZ4poFIG3NWC-Xh0_-niB6I130_provenance.
- NP651266.RA4EMTAAB3qo4P6tIZGjhDPZ4poFIG3NWC-Xh0_-niB6I130_assertion SIO_000772 10234509 NP651266.RA4EMTAAB3qo4P6tIZGjhDPZ4poFIG3NWC-Xh0_-niB6I130_provenance.
- NP651266.RA4EMTAAB3qo4P6tIZGjhDPZ4poFIG3NWC-Xh0_-niB6I130_assertion wasDerivedFrom befree-20140225 NP651266.RA4EMTAAB3qo4P6tIZGjhDPZ4poFIG3NWC-Xh0_-niB6I130_provenance.
- NP651266.RA4EMTAAB3qo4P6tIZGjhDPZ4poFIG3NWC-Xh0_-niB6I130_assertion wasGeneratedBy ECO_0000203 NP651266.RA4EMTAAB3qo4P6tIZGjhDPZ4poFIG3NWC-Xh0_-niB6I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651266.RA4EMTAAB3qo4P6tIZGjhDPZ4poFIG3NWC-Xh0_-niB6I130_provenance.