Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP385899.RAEM52Aj6nne0gclJUM0h_1VRv8Mb5gN7kEEb2rpb-xRI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP385899.RAEM52Aj6nne0gclJUM0h_1VRv8Mb5gN7kEEb2rpb-xRI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP385899.RAEM52Aj6nne0gclJUM0h_1VRv8Mb5gN7kEEb2rpb-xRI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP385899.RAEM52Aj6nne0gclJUM0h_1VRv8Mb5gN7kEEb2rpb-xRI130_provenance.
- NP385899.RAEM52Aj6nne0gclJUM0h_1VRv8Mb5gN7kEEb2rpb-xRI130_assertion description "[Pachyonychia congenita type 1 (PC-1) is an autosomal dominant ectodermal dysplasia characterized by hypertrophic nail dystrophy, focal non-epidermolytic palmoplantar keratoderma and variable features of oral leukokeratosis and follicular keratosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP385899.RAEM52Aj6nne0gclJUM0h_1VRv8Mb5gN7kEEb2rpb-xRI130_provenance.
- NP385899.RAEM52Aj6nne0gclJUM0h_1VRv8Mb5gN7kEEb2rpb-xRI130_assertion evidence source_evidence_literature NP385899.RAEM52Aj6nne0gclJUM0h_1VRv8Mb5gN7kEEb2rpb-xRI130_provenance.
- NP385899.RAEM52Aj6nne0gclJUM0h_1VRv8Mb5gN7kEEb2rpb-xRI130_assertion SIO_000772 10232400 NP385899.RAEM52Aj6nne0gclJUM0h_1VRv8Mb5gN7kEEb2rpb-xRI130_provenance.
- NP385899.RAEM52Aj6nne0gclJUM0h_1VRv8Mb5gN7kEEb2rpb-xRI130_assertion wasDerivedFrom befree-20140225 NP385899.RAEM52Aj6nne0gclJUM0h_1VRv8Mb5gN7kEEb2rpb-xRI130_provenance.
- NP385899.RAEM52Aj6nne0gclJUM0h_1VRv8Mb5gN7kEEb2rpb-xRI130_assertion wasGeneratedBy ECO_0000203 NP385899.RAEM52Aj6nne0gclJUM0h_1VRv8Mb5gN7kEEb2rpb-xRI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP385899.RAEM52Aj6nne0gclJUM0h_1VRv8Mb5gN7kEEb2rpb-xRI130_provenance.