Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP650827.RApUsDZ_ea0SJxIsUhtGI9pqVptRY0MiE4_4URh3xWw40130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP650827.RApUsDZ_ea0SJxIsUhtGI9pqVptRY0MiE4_4URh3xWw40130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650827.RApUsDZ_ea0SJxIsUhtGI9pqVptRY0MiE4_4URh3xWw40130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650827.RApUsDZ_ea0SJxIsUhtGI9pqVptRY0MiE4_4URh3xWw40130_provenance.
- NP650827.RApUsDZ_ea0SJxIsUhtGI9pqVptRY0MiE4_4URh3xWw40130_assertion description "[Microcephalic Osteodysplastic Primordial Dwarfism (MOPD) II has recently been defined as a PCNT gene defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650827.RApUsDZ_ea0SJxIsUhtGI9pqVptRY0MiE4_4URh3xWw40130_provenance.
- NP650827.RApUsDZ_ea0SJxIsUhtGI9pqVptRY0MiE4_4URh3xWw40130_assertion evidence source_evidence_literature NP650827.RApUsDZ_ea0SJxIsUhtGI9pqVptRY0MiE4_4URh3xWw40130_provenance.
- NP650827.RApUsDZ_ea0SJxIsUhtGI9pqVptRY0MiE4_4URh3xWw40130_assertion SIO_000772 23583796 NP650827.RApUsDZ_ea0SJxIsUhtGI9pqVptRY0MiE4_4URh3xWw40130_provenance.
- NP650827.RApUsDZ_ea0SJxIsUhtGI9pqVptRY0MiE4_4URh3xWw40130_assertion wasDerivedFrom befree-20140225 NP650827.RApUsDZ_ea0SJxIsUhtGI9pqVptRY0MiE4_4URh3xWw40130_provenance.
- NP650827.RApUsDZ_ea0SJxIsUhtGI9pqVptRY0MiE4_4URh3xWw40130_assertion wasGeneratedBy ECO_0000203 NP650827.RApUsDZ_ea0SJxIsUhtGI9pqVptRY0MiE4_4URh3xWw40130_provenance.
- befree-20140225 importedOn "2014-02-25" NP650827.RApUsDZ_ea0SJxIsUhtGI9pqVptRY0MiE4_4URh3xWw40130_provenance.