Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP230433.RAHAcsrMqXi91z2pDOdc6YfuJVwQMMd_G6YL6xt_vgWHc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP230433.RAHAcsrMqXi91z2pDOdc6YfuJVwQMMd_G6YL6xt_vgWHc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP230433.RAHAcsrMqXi91z2pDOdc6YfuJVwQMMd_G6YL6xt_vgWHc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP230433.RAHAcsrMqXi91z2pDOdc6YfuJVwQMMd_G6YL6xt_vgWHc130_provenance.
- NP230433.RAHAcsrMqXi91z2pDOdc6YfuJVwQMMd_G6YL6xt_vgWHc130_assertion description "[Therefore, RPE65 mutations have to be considered to cause early onset severe retinal degeneration (EOSRD), and AIPL1 mutations a form of LCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230433.RAHAcsrMqXi91z2pDOdc6YfuJVwQMMd_G6YL6xt_vgWHc130_provenance.
- NP230433.RAHAcsrMqXi91z2pDOdc6YfuJVwQMMd_G6YL6xt_vgWHc130_assertion evidence source_evidence_literature NP230433.RAHAcsrMqXi91z2pDOdc6YfuJVwQMMd_G6YL6xt_vgWHc130_provenance.
- NP230433.RAHAcsrMqXi91z2pDOdc6YfuJVwQMMd_G6YL6xt_vgWHc130_assertion SIO_000772 14611946 NP230433.RAHAcsrMqXi91z2pDOdc6YfuJVwQMMd_G6YL6xt_vgWHc130_provenance.
- NP230433.RAHAcsrMqXi91z2pDOdc6YfuJVwQMMd_G6YL6xt_vgWHc130_assertion wasDerivedFrom befree-20140225 NP230433.RAHAcsrMqXi91z2pDOdc6YfuJVwQMMd_G6YL6xt_vgWHc130_provenance.
- NP230433.RAHAcsrMqXi91z2pDOdc6YfuJVwQMMd_G6YL6xt_vgWHc130_assertion wasGeneratedBy ECO_0000203 NP230433.RAHAcsrMqXi91z2pDOdc6YfuJVwQMMd_G6YL6xt_vgWHc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP230433.RAHAcsrMqXi91z2pDOdc6YfuJVwQMMd_G6YL6xt_vgWHc130_provenance.