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- source_evidence_literature type ECO_0000212 NP669016.RA-E1cfD-IOCpW6_cTlW_16lSIhfEj46cKElP7eBNPTBw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP669016.RA-E1cfD-IOCpW6_cTlW_16lSIhfEj46cKElP7eBNPTBw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP669016.RA-E1cfD-IOCpW6_cTlW_16lSIhfEj46cKElP7eBNPTBw130_provenance.
- NP669016.RA-E1cfD-IOCpW6_cTlW_16lSIhfEj46cKElP7eBNPTBw130_assertion description "[The identification of TREX1 mutations in families with retinal vasculopathy and associated diseases such as migraine may provide new insights in migraine pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP669016.RA-E1cfD-IOCpW6_cTlW_16lSIhfEj46cKElP7eBNPTBw130_provenance.
- NP669016.RA-E1cfD-IOCpW6_cTlW_16lSIhfEj46cKElP7eBNPTBw130_assertion evidence source_evidence_literature NP669016.RA-E1cfD-IOCpW6_cTlW_16lSIhfEj46cKElP7eBNPTBw130_provenance.
- NP669016.RA-E1cfD-IOCpW6_cTlW_16lSIhfEj46cKElP7eBNPTBw130_assertion SIO_000772 18451712 NP669016.RA-E1cfD-IOCpW6_cTlW_16lSIhfEj46cKElP7eBNPTBw130_provenance.
- NP669016.RA-E1cfD-IOCpW6_cTlW_16lSIhfEj46cKElP7eBNPTBw130_assertion wasDerivedFrom befree-2016 NP669016.RA-E1cfD-IOCpW6_cTlW_16lSIhfEj46cKElP7eBNPTBw130_provenance.
- NP669016.RA-E1cfD-IOCpW6_cTlW_16lSIhfEj46cKElP7eBNPTBw130_assertion wasGeneratedBy ECO_0000203 NP669016.RA-E1cfD-IOCpW6_cTlW_16lSIhfEj46cKElP7eBNPTBw130_provenance.
- befree-2016 importedOn "2016-02-19" NP669016.RA-E1cfD-IOCpW6_cTlW_16lSIhfEj46cKElP7eBNPTBw130_provenance.