Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP381477.RAACskDWv2eiBaUkRoa3CyIDpDbeixTMExkKKsIRvBvRo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381477.RAACskDWv2eiBaUkRoa3CyIDpDbeixTMExkKKsIRvBvRo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381477.RAACskDWv2eiBaUkRoa3CyIDpDbeixTMExkKKsIRvBvRo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381477.RAACskDWv2eiBaUkRoa3CyIDpDbeixTMExkKKsIRvBvRo130_provenance.
- NP381477.RAACskDWv2eiBaUkRoa3CyIDpDbeixTMExkKKsIRvBvRo130_assertion description "[Polymorphisms at the xeroderma pigmentosum group D (XPD), excision repair cross-complementing group-1 (ERCC1) and X-ray repair cross complementing group 1 (XRCC1) genes were evaluated and correlated with clinical outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381477.RAACskDWv2eiBaUkRoa3CyIDpDbeixTMExkKKsIRvBvRo130_provenance.
- NP381477.RAACskDWv2eiBaUkRoa3CyIDpDbeixTMExkKKsIRvBvRo130_assertion evidence source_evidence_literature NP381477.RAACskDWv2eiBaUkRoa3CyIDpDbeixTMExkKKsIRvBvRo130_provenance.
- NP381477.RAACskDWv2eiBaUkRoa3CyIDpDbeixTMExkKKsIRvBvRo130_assertion SIO_000772 19443413 NP381477.RAACskDWv2eiBaUkRoa3CyIDpDbeixTMExkKKsIRvBvRo130_provenance.
- NP381477.RAACskDWv2eiBaUkRoa3CyIDpDbeixTMExkKKsIRvBvRo130_assertion wasDerivedFrom befree-20150227 NP381477.RAACskDWv2eiBaUkRoa3CyIDpDbeixTMExkKKsIRvBvRo130_provenance.
- NP381477.RAACskDWv2eiBaUkRoa3CyIDpDbeixTMExkKKsIRvBvRo130_assertion wasGeneratedBy ECO_0000203 NP381477.RAACskDWv2eiBaUkRoa3CyIDpDbeixTMExkKKsIRvBvRo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP381477.RAACskDWv2eiBaUkRoa3CyIDpDbeixTMExkKKsIRvBvRo130_provenance.