Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1075878.RAVGY67ABbl0Brs6RS5tmvQg9zh8DKjzgP-XrYFkmH_jE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1075878.RAVGY67ABbl0Brs6RS5tmvQg9zh8DKjzgP-XrYFkmH_jE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1075878.RAVGY67ABbl0Brs6RS5tmvQg9zh8DKjzgP-XrYFkmH_jE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1075878.RAVGY67ABbl0Brs6RS5tmvQg9zh8DKjzgP-XrYFkmH_jE130_provenance.
- NP1075878.RAVGY67ABbl0Brs6RS5tmvQg9zh8DKjzgP-XrYFkmH_jE130_assertion description "[Genetic polymorphisms in the 3'UTR region of the CXCL12 (rs1801157) and TP53 codon 72 (rs1042522) genes may contribute to susceptibility to childhood ALL because they affect some important processes, such as metastasis regulation and tumor suppression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1075878.RAVGY67ABbl0Brs6RS5tmvQg9zh8DKjzgP-XrYFkmH_jE130_provenance.
- NP1075878.RAVGY67ABbl0Brs6RS5tmvQg9zh8DKjzgP-XrYFkmH_jE130_assertion evidence source_evidence_literature NP1075878.RAVGY67ABbl0Brs6RS5tmvQg9zh8DKjzgP-XrYFkmH_jE130_provenance.
- NP1075878.RAVGY67ABbl0Brs6RS5tmvQg9zh8DKjzgP-XrYFkmH_jE130_assertion SIO_000772 23653000 NP1075878.RAVGY67ABbl0Brs6RS5tmvQg9zh8DKjzgP-XrYFkmH_jE130_provenance.
- NP1075878.RAVGY67ABbl0Brs6RS5tmvQg9zh8DKjzgP-XrYFkmH_jE130_assertion wasDerivedFrom befree-2016 NP1075878.RAVGY67ABbl0Brs6RS5tmvQg9zh8DKjzgP-XrYFkmH_jE130_provenance.
- NP1075878.RAVGY67ABbl0Brs6RS5tmvQg9zh8DKjzgP-XrYFkmH_jE130_assertion wasGeneratedBy ECO_0000203 NP1075878.RAVGY67ABbl0Brs6RS5tmvQg9zh8DKjzgP-XrYFkmH_jE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1075878.RAVGY67ABbl0Brs6RS5tmvQg9zh8DKjzgP-XrYFkmH_jE130_provenance.