Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP268303.RAEXyAxPydgOr8YWsebyAUO6QQ2tvFstXJZZGFOexXHKU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP268303.RAEXyAxPydgOr8YWsebyAUO6QQ2tvFstXJZZGFOexXHKU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268303.RAEXyAxPydgOr8YWsebyAUO6QQ2tvFstXJZZGFOexXHKU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268303.RAEXyAxPydgOr8YWsebyAUO6QQ2tvFstXJZZGFOexXHKU130_provenance.
- NP268303.RAEXyAxPydgOr8YWsebyAUO6QQ2tvFstXJZZGFOexXHKU130_assertion description "[Compound SFTPB 1549C-->GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268303.RAEXyAxPydgOr8YWsebyAUO6QQ2tvFstXJZZGFOexXHKU130_provenance.
- NP268303.RAEXyAxPydgOr8YWsebyAUO6QQ2tvFstXJZZGFOexXHKU130_assertion evidence source_evidence_literature NP268303.RAEXyAxPydgOr8YWsebyAUO6QQ2tvFstXJZZGFOexXHKU130_provenance.
- NP268303.RAEXyAxPydgOr8YWsebyAUO6QQ2tvFstXJZZGFOexXHKU130_assertion SIO_000772 10571948 NP268303.RAEXyAxPydgOr8YWsebyAUO6QQ2tvFstXJZZGFOexXHKU130_provenance.
- NP268303.RAEXyAxPydgOr8YWsebyAUO6QQ2tvFstXJZZGFOexXHKU130_assertion wasDerivedFrom befree-2016 NP268303.RAEXyAxPydgOr8YWsebyAUO6QQ2tvFstXJZZGFOexXHKU130_provenance.
- NP268303.RAEXyAxPydgOr8YWsebyAUO6QQ2tvFstXJZZGFOexXHKU130_assertion wasGeneratedBy ECO_0000203 NP268303.RAEXyAxPydgOr8YWsebyAUO6QQ2tvFstXJZZGFOexXHKU130_provenance.
- befree-2016 importedOn "2016-02-19" NP268303.RAEXyAxPydgOr8YWsebyAUO6QQ2tvFstXJZZGFOexXHKU130_provenance.