Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP471729.RA3TDwb-NukKrdwRutM2IdyvZJW9HkjgGWQxZ1HgwssjE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP471729.RA3TDwb-NukKrdwRutM2IdyvZJW9HkjgGWQxZ1HgwssjE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP471729.RA3TDwb-NukKrdwRutM2IdyvZJW9HkjgGWQxZ1HgwssjE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP471729.RA3TDwb-NukKrdwRutM2IdyvZJW9HkjgGWQxZ1HgwssjE130_provenance.
- NP471729.RA3TDwb-NukKrdwRutM2IdyvZJW9HkjgGWQxZ1HgwssjE130_assertion description "[In Korean women, the 399Gln polymorphism of XRCC1 is associated with an increased risk of uterine leiomyoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP471729.RA3TDwb-NukKrdwRutM2IdyvZJW9HkjgGWQxZ1HgwssjE130_provenance.
- NP471729.RA3TDwb-NukKrdwRutM2IdyvZJW9HkjgGWQxZ1HgwssjE130_assertion evidence source_evidence_literature NP471729.RA3TDwb-NukKrdwRutM2IdyvZJW9HkjgGWQxZ1HgwssjE130_provenance.
- NP471729.RA3TDwb-NukKrdwRutM2IdyvZJW9HkjgGWQxZ1HgwssjE130_assertion SIO_000772 15760950 NP471729.RA3TDwb-NukKrdwRutM2IdyvZJW9HkjgGWQxZ1HgwssjE130_provenance.
- NP471729.RA3TDwb-NukKrdwRutM2IdyvZJW9HkjgGWQxZ1HgwssjE130_assertion wasDerivedFrom befree-20140225 NP471729.RA3TDwb-NukKrdwRutM2IdyvZJW9HkjgGWQxZ1HgwssjE130_provenance.
- NP471729.RA3TDwb-NukKrdwRutM2IdyvZJW9HkjgGWQxZ1HgwssjE130_assertion wasGeneratedBy ECO_0000203 NP471729.RA3TDwb-NukKrdwRutM2IdyvZJW9HkjgGWQxZ1HgwssjE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP471729.RA3TDwb-NukKrdwRutM2IdyvZJW9HkjgGWQxZ1HgwssjE130_provenance.