Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP382198.RAmS2r3hHpqSn9cVvT9WXCC7En0Pqh4ApHBBH8jNBOlio130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP382198.RAmS2r3hHpqSn9cVvT9WXCC7En0Pqh4ApHBBH8jNBOlio130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382198.RAmS2r3hHpqSn9cVvT9WXCC7En0Pqh4ApHBBH8jNBOlio130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382198.RAmS2r3hHpqSn9cVvT9WXCC7En0Pqh4ApHBBH8jNBOlio130_provenance.
- NP382198.RAmS2r3hHpqSn9cVvT9WXCC7En0Pqh4ApHBBH8jNBOlio130_assertion description "[We conducted a case-control study to assess the role of three single-nucleotide polymorphisms (SNPs) in excision repair cross-complementation group 1 (ERCC1) and two SNPs in excision repair cross-complementation group 2 (ERCC2) on the glioma risk in a Chinese population, and investigate the gene-environmental interaction for the cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382198.RAmS2r3hHpqSn9cVvT9WXCC7En0Pqh4ApHBBH8jNBOlio130_provenance.
- NP382198.RAmS2r3hHpqSn9cVvT9WXCC7En0Pqh4ApHBBH8jNBOlio130_assertion evidence source_evidence_literature NP382198.RAmS2r3hHpqSn9cVvT9WXCC7En0Pqh4ApHBBH8jNBOlio130_provenance.
- NP382198.RAmS2r3hHpqSn9cVvT9WXCC7En0Pqh4ApHBBH8jNBOlio130_assertion SIO_000772 24782032 NP382198.RAmS2r3hHpqSn9cVvT9WXCC7En0Pqh4ApHBBH8jNBOlio130_provenance.
- NP382198.RAmS2r3hHpqSn9cVvT9WXCC7En0Pqh4ApHBBH8jNBOlio130_assertion wasDerivedFrom befree-20150227 NP382198.RAmS2r3hHpqSn9cVvT9WXCC7En0Pqh4ApHBBH8jNBOlio130_provenance.
- NP382198.RAmS2r3hHpqSn9cVvT9WXCC7En0Pqh4ApHBBH8jNBOlio130_assertion wasGeneratedBy ECO_0000203 NP382198.RAmS2r3hHpqSn9cVvT9WXCC7En0Pqh4ApHBBH8jNBOlio130_provenance.
- befree-20150227 importedOn "2015-02-27" NP382198.RAmS2r3hHpqSn9cVvT9WXCC7En0Pqh4ApHBBH8jNBOlio130_provenance.