Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP289679.RATKeTaMtFzlkoNs9PhnJ3S89sfWCAxCCq3a1nrJ7mHB0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP289679.RATKeTaMtFzlkoNs9PhnJ3S89sfWCAxCCq3a1nrJ7mHB0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP289679.RATKeTaMtFzlkoNs9PhnJ3S89sfWCAxCCq3a1nrJ7mHB0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP289679.RATKeTaMtFzlkoNs9PhnJ3S89sfWCAxCCq3a1nrJ7mHB0130_provenance.
- NP289679.RATKeTaMtFzlkoNs9PhnJ3S89sfWCAxCCq3a1nrJ7mHB0130_assertion description "[The rod domains of suprabasal keratins K1 and K10 are mutated in bullous congenital ichthyosiform erythroderma (BCIE; also called epidermolytic hyperkeratosis, EH) and mosaicism for K1/K10 mutations results in a nevoid distribution of EH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289679.RATKeTaMtFzlkoNs9PhnJ3S89sfWCAxCCq3a1nrJ7mHB0130_provenance.
- NP289679.RATKeTaMtFzlkoNs9PhnJ3S89sfWCAxCCq3a1nrJ7mHB0130_assertion evidence source_evidence_literature NP289679.RATKeTaMtFzlkoNs9PhnJ3S89sfWCAxCCq3a1nrJ7mHB0130_provenance.
- NP289679.RATKeTaMtFzlkoNs9PhnJ3S89sfWCAxCCq3a1nrJ7mHB0130_assertion SIO_000772 9028791 NP289679.RATKeTaMtFzlkoNs9PhnJ3S89sfWCAxCCq3a1nrJ7mHB0130_provenance.
- NP289679.RATKeTaMtFzlkoNs9PhnJ3S89sfWCAxCCq3a1nrJ7mHB0130_assertion wasDerivedFrom befree-20140225 NP289679.RATKeTaMtFzlkoNs9PhnJ3S89sfWCAxCCq3a1nrJ7mHB0130_provenance.
- NP289679.RATKeTaMtFzlkoNs9PhnJ3S89sfWCAxCCq3a1nrJ7mHB0130_assertion wasGeneratedBy ECO_0000203 NP289679.RATKeTaMtFzlkoNs9PhnJ3S89sfWCAxCCq3a1nrJ7mHB0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP289679.RATKeTaMtFzlkoNs9PhnJ3S89sfWCAxCCq3a1nrJ7mHB0130_provenance.