Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP556141.RAhRaEPN1FP-NTdu3yjBp7nfeByungwchHO--nxDguaV8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP556141.RAhRaEPN1FP-NTdu3yjBp7nfeByungwchHO--nxDguaV8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP556141.RAhRaEPN1FP-NTdu3yjBp7nfeByungwchHO--nxDguaV8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP556141.RAhRaEPN1FP-NTdu3yjBp7nfeByungwchHO--nxDguaV8130_provenance.
- NP556141.RAhRaEPN1FP-NTdu3yjBp7nfeByungwchHO--nxDguaV8130_assertion description "[A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556141.RAhRaEPN1FP-NTdu3yjBp7nfeByungwchHO--nxDguaV8130_provenance.
- NP556141.RAhRaEPN1FP-NTdu3yjBp7nfeByungwchHO--nxDguaV8130_assertion evidence source_evidence_literature NP556141.RAhRaEPN1FP-NTdu3yjBp7nfeByungwchHO--nxDguaV8130_provenance.
- NP556141.RAhRaEPN1FP-NTdu3yjBp7nfeByungwchHO--nxDguaV8130_assertion SIO_000772 17719747 NP556141.RAhRaEPN1FP-NTdu3yjBp7nfeByungwchHO--nxDguaV8130_provenance.
- NP556141.RAhRaEPN1FP-NTdu3yjBp7nfeByungwchHO--nxDguaV8130_assertion wasDerivedFrom befree-20140225 NP556141.RAhRaEPN1FP-NTdu3yjBp7nfeByungwchHO--nxDguaV8130_provenance.
- NP556141.RAhRaEPN1FP-NTdu3yjBp7nfeByungwchHO--nxDguaV8130_assertion wasGeneratedBy ECO_0000203 NP556141.RAhRaEPN1FP-NTdu3yjBp7nfeByungwchHO--nxDguaV8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP556141.RAhRaEPN1FP-NTdu3yjBp7nfeByungwchHO--nxDguaV8130_provenance.