Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP381828.RAIoQOOb72Rcdz1tEZbwEwNJaq1s3lMewK5XDhPUovTnE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381828.RAIoQOOb72Rcdz1tEZbwEwNJaq1s3lMewK5XDhPUovTnE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381828.RAIoQOOb72Rcdz1tEZbwEwNJaq1s3lMewK5XDhPUovTnE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381828.RAIoQOOb72Rcdz1tEZbwEwNJaq1s3lMewK5XDhPUovTnE130_provenance.
- NP381828.RAIoQOOb72Rcdz1tEZbwEwNJaq1s3lMewK5XDhPUovTnE130_assertion description "[A significant association was found between the combined heterozygous of XRCC3 and homozygous variant of XPD gene and CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381828.RAIoQOOb72Rcdz1tEZbwEwNJaq1s3lMewK5XDhPUovTnE130_provenance.
- NP381828.RAIoQOOb72Rcdz1tEZbwEwNJaq1s3lMewK5XDhPUovTnE130_assertion evidence source_evidence_literature NP381828.RAIoQOOb72Rcdz1tEZbwEwNJaq1s3lMewK5XDhPUovTnE130_provenance.
- NP381828.RAIoQOOb72Rcdz1tEZbwEwNJaq1s3lMewK5XDhPUovTnE130_assertion SIO_000772 24687779 NP381828.RAIoQOOb72Rcdz1tEZbwEwNJaq1s3lMewK5XDhPUovTnE130_provenance.
- NP381828.RAIoQOOb72Rcdz1tEZbwEwNJaq1s3lMewK5XDhPUovTnE130_assertion wasDerivedFrom befree-20150227 NP381828.RAIoQOOb72Rcdz1tEZbwEwNJaq1s3lMewK5XDhPUovTnE130_provenance.
- NP381828.RAIoQOOb72Rcdz1tEZbwEwNJaq1s3lMewK5XDhPUovTnE130_assertion wasGeneratedBy ECO_0000203 NP381828.RAIoQOOb72Rcdz1tEZbwEwNJaq1s3lMewK5XDhPUovTnE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP381828.RAIoQOOb72Rcdz1tEZbwEwNJaq1s3lMewK5XDhPUovTnE130_provenance.