Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP352157.RApKoi3aJSTr4_aZCfVM1yqSQ4sCdSu66nywL_0VMWKoM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP352157.RApKoi3aJSTr4_aZCfVM1yqSQ4sCdSu66nywL_0VMWKoM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP352157.RApKoi3aJSTr4_aZCfVM1yqSQ4sCdSu66nywL_0VMWKoM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP352157.RApKoi3aJSTr4_aZCfVM1yqSQ4sCdSu66nywL_0VMWKoM130_provenance.
- NP352157.RApKoi3aJSTr4_aZCfVM1yqSQ4sCdSu66nywL_0VMWKoM130_assertion wasGeneratedBy ECO_0000203 NP352157.RApKoi3aJSTr4_aZCfVM1yqSQ4sCdSu66nywL_0VMWKoM130_provenance.
- NP352157.RApKoi3aJSTr4_aZCfVM1yqSQ4sCdSu66nywL_0VMWKoM130_assertion wasDerivedFrom befree-20140225 NP352157.RApKoi3aJSTr4_aZCfVM1yqSQ4sCdSu66nywL_0VMWKoM130_provenance.
- NP352157.RApKoi3aJSTr4_aZCfVM1yqSQ4sCdSu66nywL_0VMWKoM130_assertion SIO_000772 17632512 NP352157.RApKoi3aJSTr4_aZCfVM1yqSQ4sCdSu66nywL_0VMWKoM130_provenance.
- NP352157.RApKoi3aJSTr4_aZCfVM1yqSQ4sCdSu66nywL_0VMWKoM130_assertion evidence source_evidence_literature NP352157.RApKoi3aJSTr4_aZCfVM1yqSQ4sCdSu66nywL_0VMWKoM130_provenance.
- NP352157.RApKoi3aJSTr4_aZCfVM1yqSQ4sCdSu66nywL_0VMWKoM130_assertion description "[By studying multiplex families, we mapped this disorder to chromosome 2q23.3-31.1 and identified LRP2 mutations in six families with Donnai-Barrow syndrome and one family with facio-oculo-acoustico-renal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352157.RApKoi3aJSTr4_aZCfVM1yqSQ4sCdSu66nywL_0VMWKoM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP352157.RApKoi3aJSTr4_aZCfVM1yqSQ4sCdSu66nywL_0VMWKoM130_provenance.