Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP152904.RAakWqX-d-KVJza3l3J8NEauKommK17R2f_fKIjHOGx5Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP152904.RAakWqX-d-KVJza3l3J8NEauKommK17R2f_fKIjHOGx5Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP152904.RAakWqX-d-KVJza3l3J8NEauKommK17R2f_fKIjHOGx5Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP152904.RAakWqX-d-KVJza3l3J8NEauKommK17R2f_fKIjHOGx5Y130_provenance.
- NP152904.RAakWqX-d-KVJza3l3J8NEauKommK17R2f_fKIjHOGx5Y130_assertion description "[distinct, heterozygous mutations (five missense, one nonsense, one deletion, and one insertion) in Darier's disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152904.RAakWqX-d-KVJza3l3J8NEauKommK17R2f_fKIjHOGx5Y130_provenance.
- NP152904.RAakWqX-d-KVJza3l3J8NEauKommK17R2f_fKIjHOGx5Y130_assertion evidence source_evidence_literature NP152904.RAakWqX-d-KVJza3l3J8NEauKommK17R2f_fKIjHOGx5Y130_provenance.
- NP152904.RAakWqX-d-KVJza3l3J8NEauKommK17R2f_fKIjHOGx5Y130_assertion SIO_000772 15186327 NP152904.RAakWqX-d-KVJza3l3J8NEauKommK17R2f_fKIjHOGx5Y130_provenance.
- NP152904.RAakWqX-d-KVJza3l3J8NEauKommK17R2f_fKIjHOGx5Y130_assertion wasDerivedFrom lhgdn-20090331 NP152904.RAakWqX-d-KVJza3l3J8NEauKommK17R2f_fKIjHOGx5Y130_provenance.
- NP152904.RAakWqX-d-KVJza3l3J8NEauKommK17R2f_fKIjHOGx5Y130_assertion wasGeneratedBy ECO_0000203 NP152904.RAakWqX-d-KVJza3l3J8NEauKommK17R2f_fKIjHOGx5Y130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP152904.RAakWqX-d-KVJza3l3J8NEauKommK17R2f_fKIjHOGx5Y130_provenance.