Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP213498.RAFnFKD6zE84Z2fSyW8rPYuCK67erWBKg5Xol9OwJU8bo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP213498.RAFnFKD6zE84Z2fSyW8rPYuCK67erWBKg5Xol9OwJU8bo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP213498.RAFnFKD6zE84Z2fSyW8rPYuCK67erWBKg5Xol9OwJU8bo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP213498.RAFnFKD6zE84Z2fSyW8rPYuCK67erWBKg5Xol9OwJU8bo130_provenance.
- NP213498.RAFnFKD6zE84Z2fSyW8rPYuCK67erWBKg5Xol9OwJU8bo130_assertion description "[Four new missense and five known mutations in K6a, one new deletion and three previously identified missense mutations in K16, plus one known mutation in K17 are reported in pachyonychia congenita.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213498.RAFnFKD6zE84Z2fSyW8rPYuCK67erWBKg5Xol9OwJU8bo130_provenance.
- NP213498.RAFnFKD6zE84Z2fSyW8rPYuCK67erWBKg5Xol9OwJU8bo130_assertion evidence source_evidence_literature NP213498.RAFnFKD6zE84Z2fSyW8rPYuCK67erWBKg5Xol9OwJU8bo130_provenance.
- NP213498.RAFnFKD6zE84Z2fSyW8rPYuCK67erWBKg5Xol9OwJU8bo130_assertion SIO_000772 17719747 NP213498.RAFnFKD6zE84Z2fSyW8rPYuCK67erWBKg5Xol9OwJU8bo130_provenance.
- NP213498.RAFnFKD6zE84Z2fSyW8rPYuCK67erWBKg5Xol9OwJU8bo130_assertion wasDerivedFrom lhgdn-20090331 NP213498.RAFnFKD6zE84Z2fSyW8rPYuCK67erWBKg5Xol9OwJU8bo130_provenance.
- NP213498.RAFnFKD6zE84Z2fSyW8rPYuCK67erWBKg5Xol9OwJU8bo130_assertion wasGeneratedBy ECO_0000203 NP213498.RAFnFKD6zE84Z2fSyW8rPYuCK67erWBKg5Xol9OwJU8bo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP213498.RAFnFKD6zE84Z2fSyW8rPYuCK67erWBKg5Xol9OwJU8bo130_provenance.