Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_provenance.
- NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_assertion wasGeneratedBy ECO_0000203 NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_provenance.
- NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_assertion wasDerivedFrom befree-20140225 NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_provenance.
- NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_assertion SIO_000772 7682883 NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_provenance.
- NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_assertion evidence source_evidence_literature NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_provenance.
- NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_assertion description "[A mutation (Met-->Arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_provenance.