Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP624201.RAr1fw9Y4G0fQeulCPDTxS-nu7woIvqFyED8QclZ3CdYo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP624201.RAr1fw9Y4G0fQeulCPDTxS-nu7woIvqFyED8QclZ3CdYo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP624201.RAr1fw9Y4G0fQeulCPDTxS-nu7woIvqFyED8QclZ3CdYo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP624201.RAr1fw9Y4G0fQeulCPDTxS-nu7woIvqFyED8QclZ3CdYo130_provenance.
- NP624201.RAr1fw9Y4G0fQeulCPDTxS-nu7woIvqFyED8QclZ3CdYo130_assertion description "[Our findings indicate a reduced NMSC risk in relation to XPD Asp312Asn and Lys751Gln variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP624201.RAr1fw9Y4G0fQeulCPDTxS-nu7woIvqFyED8QclZ3CdYo130_provenance.
- NP624201.RAr1fw9Y4G0fQeulCPDTxS-nu7woIvqFyED8QclZ3CdYo130_assertion evidence source_evidence_literature NP624201.RAr1fw9Y4G0fQeulCPDTxS-nu7woIvqFyED8QclZ3CdYo130_provenance.
- NP624201.RAr1fw9Y4G0fQeulCPDTxS-nu7woIvqFyED8QclZ3CdYo130_assertion SIO_000772 17687452 NP624201.RAr1fw9Y4G0fQeulCPDTxS-nu7woIvqFyED8QclZ3CdYo130_provenance.
- NP624201.RAr1fw9Y4G0fQeulCPDTxS-nu7woIvqFyED8QclZ3CdYo130_assertion wasDerivedFrom befree-2016 NP624201.RAr1fw9Y4G0fQeulCPDTxS-nu7woIvqFyED8QclZ3CdYo130_provenance.
- NP624201.RAr1fw9Y4G0fQeulCPDTxS-nu7woIvqFyED8QclZ3CdYo130_assertion wasGeneratedBy ECO_0000203 NP624201.RAr1fw9Y4G0fQeulCPDTxS-nu7woIvqFyED8QclZ3CdYo130_provenance.
- befree-2016 importedOn "2016-02-19" NP624201.RAr1fw9Y4G0fQeulCPDTxS-nu7woIvqFyED8QclZ3CdYo130_provenance.