Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP285493.RA-wvPLYUc12uxWQGK3GufuigQ6Q1Kuocpz-x2YN19kSE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP285493.RA-wvPLYUc12uxWQGK3GufuigQ6Q1Kuocpz-x2YN19kSE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285493.RA-wvPLYUc12uxWQGK3GufuigQ6Q1Kuocpz-x2YN19kSE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285493.RA-wvPLYUc12uxWQGK3GufuigQ6Q1Kuocpz-x2YN19kSE130_provenance.
- NP285493.RA-wvPLYUc12uxWQGK3GufuigQ6Q1Kuocpz-x2YN19kSE130_assertion description "[A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285493.RA-wvPLYUc12uxWQGK3GufuigQ6Q1Kuocpz-x2YN19kSE130_provenance.
- NP285493.RA-wvPLYUc12uxWQGK3GufuigQ6Q1Kuocpz-x2YN19kSE130_assertion evidence source_evidence_literature NP285493.RA-wvPLYUc12uxWQGK3GufuigQ6Q1Kuocpz-x2YN19kSE130_provenance.
- NP285493.RA-wvPLYUc12uxWQGK3GufuigQ6Q1Kuocpz-x2YN19kSE130_assertion SIO_000772 9653658 NP285493.RA-wvPLYUc12uxWQGK3GufuigQ6Q1Kuocpz-x2YN19kSE130_provenance.
- NP285493.RA-wvPLYUc12uxWQGK3GufuigQ6Q1Kuocpz-x2YN19kSE130_assertion wasDerivedFrom befree-20140225 NP285493.RA-wvPLYUc12uxWQGK3GufuigQ6Q1Kuocpz-x2YN19kSE130_provenance.
- NP285493.RA-wvPLYUc12uxWQGK3GufuigQ6Q1Kuocpz-x2YN19kSE130_assertion wasGeneratedBy ECO_0000203 NP285493.RA-wvPLYUc12uxWQGK3GufuigQ6Q1Kuocpz-x2YN19kSE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP285493.RA-wvPLYUc12uxWQGK3GufuigQ6Q1Kuocpz-x2YN19kSE130_provenance.