Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293353.RAwAQ7CGdM3e1fWWK0Rq7HH65_q1sgqSBLAWjKcvRVghU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1293353.RAwAQ7CGdM3e1fWWK0Rq7HH65_q1sgqSBLAWjKcvRVghU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293353.RAwAQ7CGdM3e1fWWK0Rq7HH65_q1sgqSBLAWjKcvRVghU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293353.RAwAQ7CGdM3e1fWWK0Rq7HH65_q1sgqSBLAWjKcvRVghU130_provenance.
- NP1293353.RAwAQ7CGdM3e1fWWK0Rq7HH65_q1sgqSBLAWjKcvRVghU130_assertion description "[In addition, combined inter-gene interaction analysis indicated a significant association between certain genotypes and BM, mainly involving the alleles APEX1 148Glu, IL8 -251�T and AADAT +401�T. These genotypic combinations were shown to affect cyto/chemokine levels and cell counts in CSF samples from BM patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293353.RAwAQ7CGdM3e1fWWK0Rq7HH65_q1sgqSBLAWjKcvRVghU130_provenance.
- NP1293353.RAwAQ7CGdM3e1fWWK0Rq7HH65_q1sgqSBLAWjKcvRVghU130_assertion evidence source_evidence_literature NP1293353.RAwAQ7CGdM3e1fWWK0Rq7HH65_q1sgqSBLAWjKcvRVghU130_provenance.
- NP1293353.RAwAQ7CGdM3e1fWWK0Rq7HH65_q1sgqSBLAWjKcvRVghU130_assertion SIO_000772 26316174 NP1293353.RAwAQ7CGdM3e1fWWK0Rq7HH65_q1sgqSBLAWjKcvRVghU130_provenance.
- NP1293353.RAwAQ7CGdM3e1fWWK0Rq7HH65_q1sgqSBLAWjKcvRVghU130_assertion wasDerivedFrom befree-2016 NP1293353.RAwAQ7CGdM3e1fWWK0Rq7HH65_q1sgqSBLAWjKcvRVghU130_provenance.
- NP1293353.RAwAQ7CGdM3e1fWWK0Rq7HH65_q1sgqSBLAWjKcvRVghU130_assertion wasGeneratedBy ECO_0000203 NP1293353.RAwAQ7CGdM3e1fWWK0Rq7HH65_q1sgqSBLAWjKcvRVghU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293353.RAwAQ7CGdM3e1fWWK0Rq7HH65_q1sgqSBLAWjKcvRVghU130_provenance.