Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP572318.RAEDPvqWAmo0z-BMtqsysEbTx_S94WJ2YiZLBrwsw5-Wk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP572318.RAEDPvqWAmo0z-BMtqsysEbTx_S94WJ2YiZLBrwsw5-Wk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP572318.RAEDPvqWAmo0z-BMtqsysEbTx_S94WJ2YiZLBrwsw5-Wk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP572318.RAEDPvqWAmo0z-BMtqsysEbTx_S94WJ2YiZLBrwsw5-Wk130_provenance.
- NP572318.RAEDPvqWAmo0z-BMtqsysEbTx_S94WJ2YiZLBrwsw5-Wk130_assertion description "[These results indicate that mutations in the rds gene can be expressed as a macular dystrophy, with evidence of primary cone dysfunction and preservation of peripheral rod function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP572318.RAEDPvqWAmo0z-BMtqsysEbTx_S94WJ2YiZLBrwsw5-Wk130_provenance.
- NP572318.RAEDPvqWAmo0z-BMtqsysEbTx_S94WJ2YiZLBrwsw5-Wk130_assertion evidence source_evidence_literature NP572318.RAEDPvqWAmo0z-BMtqsysEbTx_S94WJ2YiZLBrwsw5-Wk130_provenance.
- NP572318.RAEDPvqWAmo0z-BMtqsysEbTx_S94WJ2YiZLBrwsw5-Wk130_assertion SIO_000772 8302543 NP572318.RAEDPvqWAmo0z-BMtqsysEbTx_S94WJ2YiZLBrwsw5-Wk130_provenance.
- NP572318.RAEDPvqWAmo0z-BMtqsysEbTx_S94WJ2YiZLBrwsw5-Wk130_assertion wasDerivedFrom befree-20140225 NP572318.RAEDPvqWAmo0z-BMtqsysEbTx_S94WJ2YiZLBrwsw5-Wk130_provenance.
- NP572318.RAEDPvqWAmo0z-BMtqsysEbTx_S94WJ2YiZLBrwsw5-Wk130_assertion wasGeneratedBy ECO_0000203 NP572318.RAEDPvqWAmo0z-BMtqsysEbTx_S94WJ2YiZLBrwsw5-Wk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP572318.RAEDPvqWAmo0z-BMtqsysEbTx_S94WJ2YiZLBrwsw5-Wk130_provenance.