Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP754710.RAU0unkoyIM8bZ3tUHv10n4aG0-Ds3c5cuX6g378ResSI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP754710.RAU0unkoyIM8bZ3tUHv10n4aG0-Ds3c5cuX6g378ResSI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP754710.RAU0unkoyIM8bZ3tUHv10n4aG0-Ds3c5cuX6g378ResSI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP754710.RAU0unkoyIM8bZ3tUHv10n4aG0-Ds3c5cuX6g378ResSI130_provenance.
- NP754710.RAU0unkoyIM8bZ3tUHv10n4aG0-Ds3c5cuX6g378ResSI130_assertion description "[Genetic variation in p53 and ATM haplotypes and risk of glioma and meningioma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP754710.RAU0unkoyIM8bZ3tUHv10n4aG0-Ds3c5cuX6g378ResSI130_provenance.
- NP754710.RAU0unkoyIM8bZ3tUHv10n4aG0-Ds3c5cuX6g378ResSI130_assertion evidence source_evidence_literature NP754710.RAU0unkoyIM8bZ3tUHv10n4aG0-Ds3c5cuX6g378ResSI130_provenance.
- NP754710.RAU0unkoyIM8bZ3tUHv10n4aG0-Ds3c5cuX6g378ResSI130_assertion SIO_000772 17151932 NP754710.RAU0unkoyIM8bZ3tUHv10n4aG0-Ds3c5cuX6g378ResSI130_provenance.
- NP754710.RAU0unkoyIM8bZ3tUHv10n4aG0-Ds3c5cuX6g378ResSI130_assertion wasDerivedFrom befree-20150227 NP754710.RAU0unkoyIM8bZ3tUHv10n4aG0-Ds3c5cuX6g378ResSI130_provenance.
- NP754710.RAU0unkoyIM8bZ3tUHv10n4aG0-Ds3c5cuX6g378ResSI130_assertion wasGeneratedBy ECO_0000203 NP754710.RAU0unkoyIM8bZ3tUHv10n4aG0-Ds3c5cuX6g378ResSI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP754710.RAU0unkoyIM8bZ3tUHv10n4aG0-Ds3c5cuX6g378ResSI130_provenance.