Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP314234.RA7qjAhMYBLK3p2acQctiU5r269ceodlqx9o_gBao72j0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP314234.RA7qjAhMYBLK3p2acQctiU5r269ceodlqx9o_gBao72j0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP314234.RA7qjAhMYBLK3p2acQctiU5r269ceodlqx9o_gBao72j0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP314234.RA7qjAhMYBLK3p2acQctiU5r269ceodlqx9o_gBao72j0130_provenance.
- NP314234.RA7qjAhMYBLK3p2acQctiU5r269ceodlqx9o_gBao72j0130_assertion description "[The distribution of VDR genotyping in patients with SLE was 1.9% for BB (non-excisable allele homozygote), 21.78% for Bb (heterozygote), and 76.23% for bb (excisable allele homozygote).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314234.RA7qjAhMYBLK3p2acQctiU5r269ceodlqx9o_gBao72j0130_provenance.
- NP314234.RA7qjAhMYBLK3p2acQctiU5r269ceodlqx9o_gBao72j0130_assertion evidence source_evidence_literature NP314234.RA7qjAhMYBLK3p2acQctiU5r269ceodlqx9o_gBao72j0130_provenance.
- NP314234.RA7qjAhMYBLK3p2acQctiU5r269ceodlqx9o_gBao72j0130_assertion SIO_000772 16507161 NP314234.RA7qjAhMYBLK3p2acQctiU5r269ceodlqx9o_gBao72j0130_provenance.
- NP314234.RA7qjAhMYBLK3p2acQctiU5r269ceodlqx9o_gBao72j0130_assertion wasDerivedFrom befree-20140225 NP314234.RA7qjAhMYBLK3p2acQctiU5r269ceodlqx9o_gBao72j0130_provenance.
- NP314234.RA7qjAhMYBLK3p2acQctiU5r269ceodlqx9o_gBao72j0130_assertion wasGeneratedBy ECO_0000203 NP314234.RA7qjAhMYBLK3p2acQctiU5r269ceodlqx9o_gBao72j0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP314234.RA7qjAhMYBLK3p2acQctiU5r269ceodlqx9o_gBao72j0130_provenance.