Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_provenance.
- NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_assertion description "[Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_provenance.
- NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_assertion evidence source_evidence_literature NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_provenance.
- NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_assertion SIO_000772 18953341 NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_provenance.
- NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_assertion wasDerivedFrom befree-2016 NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_provenance.
- NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_assertion wasGeneratedBy ECO_0000203 NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_provenance.
- befree-2016 importedOn "2016-02-19" NP700029.RAvWVvSk2WLOSE-jVW_xRHkqN_NVMq_5dF-0RcFGIzDIg130_provenance.