Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP849443.RA906K9IhbIVkU21P7eqp1_Rm12PASWGbViGpJNEuCsGA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP849443.RA906K9IhbIVkU21P7eqp1_Rm12PASWGbViGpJNEuCsGA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP849443.RA906K9IhbIVkU21P7eqp1_Rm12PASWGbViGpJNEuCsGA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP849443.RA906K9IhbIVkU21P7eqp1_Rm12PASWGbViGpJNEuCsGA130_provenance.
- NP849443.RA906K9IhbIVkU21P7eqp1_Rm12PASWGbViGpJNEuCsGA130_assertion description "[These data indicate that carriage of the less frequent allele of the Taq I RFLP (t) in the VDR gene significantly increases the risk of developing L-EOP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP849443.RA906K9IhbIVkU21P7eqp1_Rm12PASWGbViGpJNEuCsGA130_provenance.
- NP849443.RA906K9IhbIVkU21P7eqp1_Rm12PASWGbViGpJNEuCsGA130_assertion evidence source_evidence_literature NP849443.RA906K9IhbIVkU21P7eqp1_Rm12PASWGbViGpJNEuCsGA130_provenance.
- NP849443.RA906K9IhbIVkU21P7eqp1_Rm12PASWGbViGpJNEuCsGA130_assertion SIO_000772 10505806 NP849443.RA906K9IhbIVkU21P7eqp1_Rm12PASWGbViGpJNEuCsGA130_provenance.
- NP849443.RA906K9IhbIVkU21P7eqp1_Rm12PASWGbViGpJNEuCsGA130_assertion wasDerivedFrom befree-20140225 NP849443.RA906K9IhbIVkU21P7eqp1_Rm12PASWGbViGpJNEuCsGA130_provenance.
- NP849443.RA906K9IhbIVkU21P7eqp1_Rm12PASWGbViGpJNEuCsGA130_assertion wasGeneratedBy ECO_0000203 NP849443.RA906K9IhbIVkU21P7eqp1_Rm12PASWGbViGpJNEuCsGA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP849443.RA906K9IhbIVkU21P7eqp1_Rm12PASWGbViGpJNEuCsGA130_provenance.