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- source_evidence_literature type ECO_0000212 NP898229.RAp3NU8-RUWJZ_6GqiWwPZhQ366bS37BDkTHn4Y9WXmnk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP898229.RAp3NU8-RUWJZ_6GqiWwPZhQ366bS37BDkTHn4Y9WXmnk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP898229.RAp3NU8-RUWJZ_6GqiWwPZhQ366bS37BDkTHn4Y9WXmnk130_provenance.
- NP898229.RAp3NU8-RUWJZ_6GqiWwPZhQ366bS37BDkTHn4Y9WXmnk130_assertion description "[We conclude that variant MBL2 structural genotype constitutes a significant risk factor for reactive amyloidosis in RA and that the increased risk is probably related to MBL-mediated impairment of mononuclear phagocyte function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898229.RAp3NU8-RUWJZ_6GqiWwPZhQ366bS37BDkTHn4Y9WXmnk130_provenance.
- NP898229.RAp3NU8-RUWJZ_6GqiWwPZhQ366bS37BDkTHn4Y9WXmnk130_assertion evidence source_evidence_literature NP898229.RAp3NU8-RUWJZ_6GqiWwPZhQ366bS37BDkTHn4Y9WXmnk130_provenance.
- NP898229.RAp3NU8-RUWJZ_6GqiWwPZhQ366bS37BDkTHn4Y9WXmnk130_assertion SIO_000772 17875183 NP898229.RAp3NU8-RUWJZ_6GqiWwPZhQ366bS37BDkTHn4Y9WXmnk130_provenance.
- NP898229.RAp3NU8-RUWJZ_6GqiWwPZhQ366bS37BDkTHn4Y9WXmnk130_assertion wasDerivedFrom befree-20150227 NP898229.RAp3NU8-RUWJZ_6GqiWwPZhQ366bS37BDkTHn4Y9WXmnk130_provenance.
- NP898229.RAp3NU8-RUWJZ_6GqiWwPZhQ366bS37BDkTHn4Y9WXmnk130_assertion wasGeneratedBy ECO_0000203 NP898229.RAp3NU8-RUWJZ_6GqiWwPZhQ366bS37BDkTHn4Y9WXmnk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP898229.RAp3NU8-RUWJZ_6GqiWwPZhQ366bS37BDkTHn4Y9WXmnk130_provenance.