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- source_evidence_literature type ECO_0000212 NP1093699.RA_ZhULlKBDt5HOfkJLIh1s1_WLjTGKaSgkpJQWQI3MFw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1093699.RA_ZhULlKBDt5HOfkJLIh1s1_WLjTGKaSgkpJQWQI3MFw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1093699.RA_ZhULlKBDt5HOfkJLIh1s1_WLjTGKaSgkpJQWQI3MFw130_provenance.
- NP1093699.RA_ZhULlKBDt5HOfkJLIh1s1_WLjTGKaSgkpJQWQI3MFw130_assertion description "[VWD is classified into quantitative deficiencies of VWF (type 1 and type 3 VWD) and qualitative variants (type 2 VWD), because of a dysfunctional VWF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1093699.RA_ZhULlKBDt5HOfkJLIh1s1_WLjTGKaSgkpJQWQI3MFw130_provenance.
- NP1093699.RA_ZhULlKBDt5HOfkJLIh1s1_WLjTGKaSgkpJQWQI3MFw130_assertion evidence source_evidence_literature NP1093699.RA_ZhULlKBDt5HOfkJLIh1s1_WLjTGKaSgkpJQWQI3MFw130_provenance.
- NP1093699.RA_ZhULlKBDt5HOfkJLIh1s1_WLjTGKaSgkpJQWQI3MFw130_assertion SIO_000772 23852183 NP1093699.RA_ZhULlKBDt5HOfkJLIh1s1_WLjTGKaSgkpJQWQI3MFw130_provenance.
- NP1093699.RA_ZhULlKBDt5HOfkJLIh1s1_WLjTGKaSgkpJQWQI3MFw130_assertion wasDerivedFrom befree-2016 NP1093699.RA_ZhULlKBDt5HOfkJLIh1s1_WLjTGKaSgkpJQWQI3MFw130_provenance.
- NP1093699.RA_ZhULlKBDt5HOfkJLIh1s1_WLjTGKaSgkpJQWQI3MFw130_assertion wasGeneratedBy ECO_0000203 NP1093699.RA_ZhULlKBDt5HOfkJLIh1s1_WLjTGKaSgkpJQWQI3MFw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1093699.RA_ZhULlKBDt5HOfkJLIh1s1_WLjTGKaSgkpJQWQI3MFw130_provenance.