Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP544759.RAYYLKiUM1j_V6HaKgzPWyv7Fm3mEVEtYE7dm_kvndafs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP544759.RAYYLKiUM1j_V6HaKgzPWyv7Fm3mEVEtYE7dm_kvndafs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP544759.RAYYLKiUM1j_V6HaKgzPWyv7Fm3mEVEtYE7dm_kvndafs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP544759.RAYYLKiUM1j_V6HaKgzPWyv7Fm3mEVEtYE7dm_kvndafs130_provenance.
- NP544759.RAYYLKiUM1j_V6HaKgzPWyv7Fm3mEVEtYE7dm_kvndafs130_assertion description "[Common variants (MAF > 2%) were included in a case-control association analysis that showed significant association after multiple testing correction of two SNPs located in the promoter region of AANAT with MD: rs3760138 (P = 0.00006) and rs4238989 (P = 0.005).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP544759.RAYYLKiUM1j_V6HaKgzPWyv7Fm3mEVEtYE7dm_kvndafs130_provenance.
- NP544759.RAYYLKiUM1j_V6HaKgzPWyv7Fm3mEVEtYE7dm_kvndafs130_assertion evidence source_evidence_literature NP544759.RAYYLKiUM1j_V6HaKgzPWyv7Fm3mEVEtYE7dm_kvndafs130_provenance.
- NP544759.RAYYLKiUM1j_V6HaKgzPWyv7Fm3mEVEtYE7dm_kvndafs130_assertion SIO_000772 20459461 NP544759.RAYYLKiUM1j_V6HaKgzPWyv7Fm3mEVEtYE7dm_kvndafs130_provenance.
- NP544759.RAYYLKiUM1j_V6HaKgzPWyv7Fm3mEVEtYE7dm_kvndafs130_assertion wasDerivedFrom befree-20150227 NP544759.RAYYLKiUM1j_V6HaKgzPWyv7Fm3mEVEtYE7dm_kvndafs130_provenance.
- NP544759.RAYYLKiUM1j_V6HaKgzPWyv7Fm3mEVEtYE7dm_kvndafs130_assertion wasGeneratedBy ECO_0000203 NP544759.RAYYLKiUM1j_V6HaKgzPWyv7Fm3mEVEtYE7dm_kvndafs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP544759.RAYYLKiUM1j_V6HaKgzPWyv7Fm3mEVEtYE7dm_kvndafs130_provenance.