Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP865076.RAkpGEPkTAe7qoFEpsrVEaSJ4F7hv0t3qc-gv96x2kjEk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP865076.RAkpGEPkTAe7qoFEpsrVEaSJ4F7hv0t3qc-gv96x2kjEk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865076.RAkpGEPkTAe7qoFEpsrVEaSJ4F7hv0t3qc-gv96x2kjEk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865076.RAkpGEPkTAe7qoFEpsrVEaSJ4F7hv0t3qc-gv96x2kjEk130_provenance.
- NP865076.RAkpGEPkTAe7qoFEpsrVEaSJ4F7hv0t3qc-gv96x2kjEk130_assertion description "[We previously reported the linkage signals on chromosomes 1, 7, and 17 in Caucasian families with generalized vitiligo and associated autoimmune diseases and identified the risk loci of chromosomes 17 and 1 as NLRP1 (NALP1) and FOXD3, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865076.RAkpGEPkTAe7qoFEpsrVEaSJ4F7hv0t3qc-gv96x2kjEk130_provenance.
- NP865076.RAkpGEPkTAe7qoFEpsrVEaSJ4F7hv0t3qc-gv96x2kjEk130_assertion evidence source_evidence_literature NP865076.RAkpGEPkTAe7qoFEpsrVEaSJ4F7hv0t3qc-gv96x2kjEk130_provenance.
- NP865076.RAkpGEPkTAe7qoFEpsrVEaSJ4F7hv0t3qc-gv96x2kjEk130_assertion SIO_000772 19727120 NP865076.RAkpGEPkTAe7qoFEpsrVEaSJ4F7hv0t3qc-gv96x2kjEk130_provenance.
- NP865076.RAkpGEPkTAe7qoFEpsrVEaSJ4F7hv0t3qc-gv96x2kjEk130_assertion wasDerivedFrom befree-20150227 NP865076.RAkpGEPkTAe7qoFEpsrVEaSJ4F7hv0t3qc-gv96x2kjEk130_provenance.
- NP865076.RAkpGEPkTAe7qoFEpsrVEaSJ4F7hv0t3qc-gv96x2kjEk130_assertion wasGeneratedBy ECO_0000203 NP865076.RAkpGEPkTAe7qoFEpsrVEaSJ4F7hv0t3qc-gv96x2kjEk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP865076.RAkpGEPkTAe7qoFEpsrVEaSJ4F7hv0t3qc-gv96x2kjEk130_provenance.