Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP426473.RAK1NV30qc4xTtjEuOPB42ASZwLG63FYkrYTWBma55Rlk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426473.RAK1NV30qc4xTtjEuOPB42ASZwLG63FYkrYTWBma55Rlk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426473.RAK1NV30qc4xTtjEuOPB42ASZwLG63FYkrYTWBma55Rlk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426473.RAK1NV30qc4xTtjEuOPB42ASZwLG63FYkrYTWBma55Rlk130_provenance.
- NP426473.RAK1NV30qc4xTtjEuOPB42ASZwLG63FYkrYTWBma55Rlk130_assertion description "[It has recently been demonstrated that genetic defects in keratin genes cause a number of different skin disorders, including epidermolysis bullosa simplex (EBS), epidermolytic hyperkeratosis (EH), the EH form of epidermal nevi, epidermolytic and non-epidermolytic forms of palmoplantar keratoderma (EPPK and PPK) and pachyonychia congenita (PC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426473.RAK1NV30qc4xTtjEuOPB42ASZwLG63FYkrYTWBma55Rlk130_provenance.
- NP426473.RAK1NV30qc4xTtjEuOPB42ASZwLG63FYkrYTWBma55Rlk130_assertion evidence source_evidence_literature NP426473.RAK1NV30qc4xTtjEuOPB42ASZwLG63FYkrYTWBma55Rlk130_provenance.
- NP426473.RAK1NV30qc4xTtjEuOPB42ASZwLG63FYkrYTWBma55Rlk130_assertion SIO_000772 9023700 NP426473.RAK1NV30qc4xTtjEuOPB42ASZwLG63FYkrYTWBma55Rlk130_provenance.
- NP426473.RAK1NV30qc4xTtjEuOPB42ASZwLG63FYkrYTWBma55Rlk130_assertion wasDerivedFrom befree-20150227 NP426473.RAK1NV30qc4xTtjEuOPB42ASZwLG63FYkrYTWBma55Rlk130_provenance.
- NP426473.RAK1NV30qc4xTtjEuOPB42ASZwLG63FYkrYTWBma55Rlk130_assertion wasGeneratedBy ECO_0000203 NP426473.RAK1NV30qc4xTtjEuOPB42ASZwLG63FYkrYTWBma55Rlk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426473.RAK1NV30qc4xTtjEuOPB42ASZwLG63FYkrYTWBma55Rlk130_provenance.