Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP464850.RAdQ2CgkANNJd4gMouooFVoU-bS6gfk8C_bHHHQ6IeWyk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP464850.RAdQ2CgkANNJd4gMouooFVoU-bS6gfk8C_bHHHQ6IeWyk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP464850.RAdQ2CgkANNJd4gMouooFVoU-bS6gfk8C_bHHHQ6IeWyk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP464850.RAdQ2CgkANNJd4gMouooFVoU-bS6gfk8C_bHHHQ6IeWyk130_provenance.
- NP464850.RAdQ2CgkANNJd4gMouooFVoU-bS6gfk8C_bHHHQ6IeWyk130_assertion wasGeneratedBy ECO_0000203 NP464850.RAdQ2CgkANNJd4gMouooFVoU-bS6gfk8C_bHHHQ6IeWyk130_provenance.
- NP464850.RAdQ2CgkANNJd4gMouooFVoU-bS6gfk8C_bHHHQ6IeWyk130_assertion wasDerivedFrom befree-20140225 NP464850.RAdQ2CgkANNJd4gMouooFVoU-bS6gfk8C_bHHHQ6IeWyk130_provenance.
- NP464850.RAdQ2CgkANNJd4gMouooFVoU-bS6gfk8C_bHHHQ6IeWyk130_assertion SIO_000772 23171239 NP464850.RAdQ2CgkANNJd4gMouooFVoU-bS6gfk8C_bHHHQ6IeWyk130_provenance.
- NP464850.RAdQ2CgkANNJd4gMouooFVoU-bS6gfk8C_bHHHQ6IeWyk130_assertion evidence source_evidence_literature NP464850.RAdQ2CgkANNJd4gMouooFVoU-bS6gfk8C_bHHHQ6IeWyk130_provenance.
- NP464850.RAdQ2CgkANNJd4gMouooFVoU-bS6gfk8C_bHHHQ6IeWyk130_assertion description "[Severe congenital neutropenia type 4 (SCN4) is an autosomal recessive disorder caused by mutations in the third subunit of the enzyme glucose-6-phosphatase (G6PC3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP464850.RAdQ2CgkANNJd4gMouooFVoU-bS6gfk8C_bHHHQ6IeWyk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP464850.RAdQ2CgkANNJd4gMouooFVoU-bS6gfk8C_bHHHQ6IeWyk130_provenance.