Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP555295.RASanlSt48AVXs1LffA-_-Kbo4TPqURP2dgNVeW-CeQwQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP555295.RASanlSt48AVXs1LffA-_-Kbo4TPqURP2dgNVeW-CeQwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP555295.RASanlSt48AVXs1LffA-_-Kbo4TPqURP2dgNVeW-CeQwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP555295.RASanlSt48AVXs1LffA-_-Kbo4TPqURP2dgNVeW-CeQwQ130_provenance.
- NP555295.RASanlSt48AVXs1LffA-_-Kbo4TPqURP2dgNVeW-CeQwQ130_assertion description "[We report an unusual case of an inherited disorder of the desmosomal protein plakophilin 1, resulting in ectodermal dysplasia-skin fragility syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP555295.RASanlSt48AVXs1LffA-_-Kbo4TPqURP2dgNVeW-CeQwQ130_provenance.
- NP555295.RASanlSt48AVXs1LffA-_-Kbo4TPqURP2dgNVeW-CeQwQ130_assertion evidence source_evidence_literature NP555295.RASanlSt48AVXs1LffA-_-Kbo4TPqURP2dgNVeW-CeQwQ130_provenance.
- NP555295.RASanlSt48AVXs1LffA-_-Kbo4TPqURP2dgNVeW-CeQwQ130_assertion SIO_000772 16781314 NP555295.RASanlSt48AVXs1LffA-_-Kbo4TPqURP2dgNVeW-CeQwQ130_provenance.
- NP555295.RASanlSt48AVXs1LffA-_-Kbo4TPqURP2dgNVeW-CeQwQ130_assertion wasDerivedFrom befree-2016 NP555295.RASanlSt48AVXs1LffA-_-Kbo4TPqURP2dgNVeW-CeQwQ130_provenance.
- NP555295.RASanlSt48AVXs1LffA-_-Kbo4TPqURP2dgNVeW-CeQwQ130_assertion wasGeneratedBy ECO_0000203 NP555295.RASanlSt48AVXs1LffA-_-Kbo4TPqURP2dgNVeW-CeQwQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP555295.RASanlSt48AVXs1LffA-_-Kbo4TPqURP2dgNVeW-CeQwQ130_provenance.