Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_provenance.
- NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_assertion description "[Highlights of the efforts in the past year include the identification of mutations in an epidermal transglutaminase gene in lamellar ichthyosis as well as mutations in an additional five keratin genes causing four different abnormal phenotypes, and mutations in beta 4 integrin and bullous pemphigoid antigen 2 genes in junctional epidermolysis bullosa and in the p16NK-4a gene in 50% of kindreds with familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_provenance.
- NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_assertion evidence source_evidence_literature NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_provenance.
- NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_assertion SIO_000772 8791519 NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_provenance.
- NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_assertion wasDerivedFrom befree-20150227 NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_provenance.
- NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_assertion wasGeneratedBy ECO_0000203 NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP841746.RAdcDY1EEVeWb3nGsW0G8g1ZGntTaJxwCnyESK7IUl9Hs130_provenance.