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- source_evidence_literature type ECO_0000212 NP672269.RACLrylDIb6nruFuHaSBF91lil3zR83KE7m-8YYLO8Ihw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP672269.RACLrylDIb6nruFuHaSBF91lil3zR83KE7m-8YYLO8Ihw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP672269.RACLrylDIb6nruFuHaSBF91lil3zR83KE7m-8YYLO8Ihw130_provenance.
- NP672269.RACLrylDIb6nruFuHaSBF91lil3zR83KE7m-8YYLO8Ihw130_assertion description "[We also revealed that mutations in RLBP1 may lead to FAP with cone dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672269.RACLrylDIb6nruFuHaSBF91lil3zR83KE7m-8YYLO8Ihw130_provenance.
- NP672269.RACLrylDIb6nruFuHaSBF91lil3zR83KE7m-8YYLO8Ihw130_assertion evidence source_evidence_literature NP672269.RACLrylDIb6nruFuHaSBF91lil3zR83KE7m-8YYLO8Ihw130_provenance.
- NP672269.RACLrylDIb6nruFuHaSBF91lil3zR83KE7m-8YYLO8Ihw130_assertion SIO_000772 22559933 NP672269.RACLrylDIb6nruFuHaSBF91lil3zR83KE7m-8YYLO8Ihw130_provenance.
- NP672269.RACLrylDIb6nruFuHaSBF91lil3zR83KE7m-8YYLO8Ihw130_assertion wasDerivedFrom befree-20150227 NP672269.RACLrylDIb6nruFuHaSBF91lil3zR83KE7m-8YYLO8Ihw130_provenance.
- NP672269.RACLrylDIb6nruFuHaSBF91lil3zR83KE7m-8YYLO8Ihw130_assertion wasGeneratedBy ECO_0000203 NP672269.RACLrylDIb6nruFuHaSBF91lil3zR83KE7m-8YYLO8Ihw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP672269.RACLrylDIb6nruFuHaSBF91lil3zR83KE7m-8YYLO8Ihw130_provenance.