Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP139264.RAhpPgI0ZD-lUQRKpYIlB0ecC65H7NdF-B1gRQ_-q3utg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP139264.RAhpPgI0ZD-lUQRKpYIlB0ecC65H7NdF-B1gRQ_-q3utg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP139264.RAhpPgI0ZD-lUQRKpYIlB0ecC65H7NdF-B1gRQ_-q3utg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP139264.RAhpPgI0ZD-lUQRKpYIlB0ecC65H7NdF-B1gRQ_-q3utg130_provenance.
- NP139264.RAhpPgI0ZD-lUQRKpYIlB0ecC65H7NdF-B1gRQ_-q3utg130_assertion description "[However, the carrier frequency of the GSTP1 Val(105) allele in combined cutaneous LE (SCLE and DLE) patients with PLE was 42%, significantly lower than in those without PLE (72%), which did survive correction (corrected P=0.043).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP139264.RAhpPgI0ZD-lUQRKpYIlB0ecC65H7NdF-B1gRQ_-q3utg130_provenance.
- NP139264.RAhpPgI0ZD-lUQRKpYIlB0ecC65H7NdF-B1gRQ_-q3utg130_assertion evidence source_evidence_literature NP139264.RAhpPgI0ZD-lUQRKpYIlB0ecC65H7NdF-B1gRQ_-q3utg130_provenance.
- NP139264.RAhpPgI0ZD-lUQRKpYIlB0ecC65H7NdF-B1gRQ_-q3utg130_assertion SIO_000772 18288203 NP139264.RAhpPgI0ZD-lUQRKpYIlB0ecC65H7NdF-B1gRQ_-q3utg130_provenance.
- NP139264.RAhpPgI0ZD-lUQRKpYIlB0ecC65H7NdF-B1gRQ_-q3utg130_assertion wasDerivedFrom gad-20150221 NP139264.RAhpPgI0ZD-lUQRKpYIlB0ecC65H7NdF-B1gRQ_-q3utg130_provenance.
- NP139264.RAhpPgI0ZD-lUQRKpYIlB0ecC65H7NdF-B1gRQ_-q3utg130_assertion wasGeneratedBy ECO_0000203 NP139264.RAhpPgI0ZD-lUQRKpYIlB0ecC65H7NdF-B1gRQ_-q3utg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP139264.RAhpPgI0ZD-lUQRKpYIlB0ecC65H7NdF-B1gRQ_-q3utg130_provenance.