Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP761022.RATdFVLa_IqRRcbI7xNfU3YZE5_8hStmpElp_1_SGNu74130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP761022.RATdFVLa_IqRRcbI7xNfU3YZE5_8hStmpElp_1_SGNu74130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761022.RATdFVLa_IqRRcbI7xNfU3YZE5_8hStmpElp_1_SGNu74130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761022.RATdFVLa_IqRRcbI7xNfU3YZE5_8hStmpElp_1_SGNu74130_provenance.
- NP761022.RATdFVLa_IqRRcbI7xNfU3YZE5_8hStmpElp_1_SGNu74130_assertion description "[The purpose of this study was to determine the prevalence of mutations in the peripherin/RDS gene in Spanish patients with different types of autosomal dominant macular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761022.RATdFVLa_IqRRcbI7xNfU3YZE5_8hStmpElp_1_SGNu74130_provenance.
- NP761022.RATdFVLa_IqRRcbI7xNfU3YZE5_8hStmpElp_1_SGNu74130_assertion evidence source_evidence_literature NP761022.RATdFVLa_IqRRcbI7xNfU3YZE5_8hStmpElp_1_SGNu74130_provenance.
- NP761022.RATdFVLa_IqRRcbI7xNfU3YZE5_8hStmpElp_1_SGNu74130_assertion SIO_000772 17653047 NP761022.RATdFVLa_IqRRcbI7xNfU3YZE5_8hStmpElp_1_SGNu74130_provenance.
- NP761022.RATdFVLa_IqRRcbI7xNfU3YZE5_8hStmpElp_1_SGNu74130_assertion wasDerivedFrom befree-20150227 NP761022.RATdFVLa_IqRRcbI7xNfU3YZE5_8hStmpElp_1_SGNu74130_provenance.
- NP761022.RATdFVLa_IqRRcbI7xNfU3YZE5_8hStmpElp_1_SGNu74130_assertion wasGeneratedBy ECO_0000203 NP761022.RATdFVLa_IqRRcbI7xNfU3YZE5_8hStmpElp_1_SGNu74130_provenance.
- befree-20150227 importedOn "2015-02-27" NP761022.RATdFVLa_IqRRcbI7xNfU3YZE5_8hStmpElp_1_SGNu74130_provenance.