Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP71764.RAQUZRWYH6FVzHMl9xeE3X_jIf0TQQEjqvF3OzFtvMqPA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP71764.RAQUZRWYH6FVzHMl9xeE3X_jIf0TQQEjqvF3OzFtvMqPA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP71764.RAQUZRWYH6FVzHMl9xeE3X_jIf0TQQEjqvF3OzFtvMqPA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP71764.RAQUZRWYH6FVzHMl9xeE3X_jIf0TQQEjqvF3OzFtvMqPA130_provenance.
- NP71764.RAQUZRWYH6FVzHMl9xeE3X_jIf0TQQEjqvF3OzFtvMqPA130_assertion description "[ Identification of mild or intermediate mutations causing HPA could provide fast and reliable information about future clinical outcome of a newborn infant. Molecular diagnosis of HPA should be preceded by biochemical analysis and implemented to different]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP71764.RAQUZRWYH6FVzHMl9xeE3X_jIf0TQQEjqvF3OzFtvMqPA130_provenance.
- NP71764.RAQUZRWYH6FVzHMl9xeE3X_jIf0TQQEjqvF3OzFtvMqPA130_assertion evidence source_evidence_literature NP71764.RAQUZRWYH6FVzHMl9xeE3X_jIf0TQQEjqvF3OzFtvMqPA130_provenance.
- NP71764.RAQUZRWYH6FVzHMl9xeE3X_jIf0TQQEjqvF3OzFtvMqPA130_assertion SIO_000772 11678552 NP71764.RAQUZRWYH6FVzHMl9xeE3X_jIf0TQQEjqvF3OzFtvMqPA130_provenance.
- NP71764.RAQUZRWYH6FVzHMl9xeE3X_jIf0TQQEjqvF3OzFtvMqPA130_assertion wasDerivedFrom gad-20150221 NP71764.RAQUZRWYH6FVzHMl9xeE3X_jIf0TQQEjqvF3OzFtvMqPA130_provenance.
- NP71764.RAQUZRWYH6FVzHMl9xeE3X_jIf0TQQEjqvF3OzFtvMqPA130_assertion wasGeneratedBy ECO_0000203 NP71764.RAQUZRWYH6FVzHMl9xeE3X_jIf0TQQEjqvF3OzFtvMqPA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP71764.RAQUZRWYH6FVzHMl9xeE3X_jIf0TQQEjqvF3OzFtvMqPA130_provenance.