Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP382026.RAhhFoCWPADsvHNSHdwR1qwlUd5IfQT_na_47uHEK7UwM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP382026.RAhhFoCWPADsvHNSHdwR1qwlUd5IfQT_na_47uHEK7UwM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382026.RAhhFoCWPADsvHNSHdwR1qwlUd5IfQT_na_47uHEK7UwM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382026.RAhhFoCWPADsvHNSHdwR1qwlUd5IfQT_na_47uHEK7UwM130_provenance.
- NP382026.RAhhFoCWPADsvHNSHdwR1qwlUd5IfQT_na_47uHEK7UwM130_assertion description "[Proportions of XPD codon 312( *)GG/GA/AA, XPD codon 751( *)TT/TG/GG, and XPD promoter -114( *)GG/GC/CC were [1] 65%/22.5%/12.5%, 92.5%/6.7%/0.8%, and 22.5%/46.7%/30.8%; and [2] 64.3%/22.3%/13.4%, 92%/7.1%/0.9%, and 23.2%/46.4%/30.4%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382026.RAhhFoCWPADsvHNSHdwR1qwlUd5IfQT_na_47uHEK7UwM130_provenance.
- NP382026.RAhhFoCWPADsvHNSHdwR1qwlUd5IfQT_na_47uHEK7UwM130_assertion evidence source_evidence_literature NP382026.RAhhFoCWPADsvHNSHdwR1qwlUd5IfQT_na_47uHEK7UwM130_provenance.
- NP382026.RAhhFoCWPADsvHNSHdwR1qwlUd5IfQT_na_47uHEK7UwM130_assertion SIO_000772 18177646 NP382026.RAhhFoCWPADsvHNSHdwR1qwlUd5IfQT_na_47uHEK7UwM130_provenance.
- NP382026.RAhhFoCWPADsvHNSHdwR1qwlUd5IfQT_na_47uHEK7UwM130_assertion wasDerivedFrom befree-20150227 NP382026.RAhhFoCWPADsvHNSHdwR1qwlUd5IfQT_na_47uHEK7UwM130_provenance.
- NP382026.RAhhFoCWPADsvHNSHdwR1qwlUd5IfQT_na_47uHEK7UwM130_assertion wasGeneratedBy ECO_0000203 NP382026.RAhhFoCWPADsvHNSHdwR1qwlUd5IfQT_na_47uHEK7UwM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP382026.RAhhFoCWPADsvHNSHdwR1qwlUd5IfQT_na_47uHEK7UwM130_provenance.