Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP407604.RAkVf1sn7jO_B7KXKGNM5blwVWo_nzxiMGdneL8lIVuJE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP407604.RAkVf1sn7jO_B7KXKGNM5blwVWo_nzxiMGdneL8lIVuJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP407604.RAkVf1sn7jO_B7KXKGNM5blwVWo_nzxiMGdneL8lIVuJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP407604.RAkVf1sn7jO_B7KXKGNM5blwVWo_nzxiMGdneL8lIVuJE130_provenance.
- NP407604.RAkVf1sn7jO_B7KXKGNM5blwVWo_nzxiMGdneL8lIVuJE130_assertion description "[These SNPs are in or near genes that are highly expressed in the brain (HECW2, HIP1, BIN2, GRIA1), genes involved in neural development and function (KCNQ4, LMO4, GRIA1, NETO1) and autophagy (ATG4C), and genes that are associated with risk of various diseases including cancer and Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP407604.RAkVf1sn7jO_B7KXKGNM5blwVWo_nzxiMGdneL8lIVuJE130_provenance.
- NP407604.RAkVf1sn7jO_B7KXKGNM5blwVWo_nzxiMGdneL8lIVuJE130_assertion evidence source_evidence_literature NP407604.RAkVf1sn7jO_B7KXKGNM5blwVWo_nzxiMGdneL8lIVuJE130_provenance.
- NP407604.RAkVf1sn7jO_B7KXKGNM5blwVWo_nzxiMGdneL8lIVuJE130_assertion SIO_000772 21782286 NP407604.RAkVf1sn7jO_B7KXKGNM5blwVWo_nzxiMGdneL8lIVuJE130_provenance.
- NP407604.RAkVf1sn7jO_B7KXKGNM5blwVWo_nzxiMGdneL8lIVuJE130_assertion wasDerivedFrom befree-20140225 NP407604.RAkVf1sn7jO_B7KXKGNM5blwVWo_nzxiMGdneL8lIVuJE130_provenance.
- NP407604.RAkVf1sn7jO_B7KXKGNM5blwVWo_nzxiMGdneL8lIVuJE130_assertion wasGeneratedBy ECO_0000203 NP407604.RAkVf1sn7jO_B7KXKGNM5blwVWo_nzxiMGdneL8lIVuJE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP407604.RAkVf1sn7jO_B7KXKGNM5blwVWo_nzxiMGdneL8lIVuJE130_provenance.