Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP373201.RAnN0URdTS_8qq-T1pXSqb2sHHaDx3ONocKv0sZLnAy_4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP373201.RAnN0URdTS_8qq-T1pXSqb2sHHaDx3ONocKv0sZLnAy_4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP373201.RAnN0URdTS_8qq-T1pXSqb2sHHaDx3ONocKv0sZLnAy_4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP373201.RAnN0URdTS_8qq-T1pXSqb2sHHaDx3ONocKv0sZLnAy_4130_provenance.
- NP373201.RAnN0URdTS_8qq-T1pXSqb2sHHaDx3ONocKv0sZLnAy_4130_assertion description "[Functional deficiency or absence of the human von Willebrand factor (VWF)-cleaving protease (VWF-cp), recently termed ADAMTS13, has been shown to cause acquired and congenital thrombotic thrombocytopenic purpura (TTP), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP373201.RAnN0URdTS_8qq-T1pXSqb2sHHaDx3ONocKv0sZLnAy_4130_provenance.
- NP373201.RAnN0URdTS_8qq-T1pXSqb2sHHaDx3ONocKv0sZLnAy_4130_assertion evidence source_evidence_literature NP373201.RAnN0URdTS_8qq-T1pXSqb2sHHaDx3ONocKv0sZLnAy_4130_provenance.
- NP373201.RAnN0URdTS_8qq-T1pXSqb2sHHaDx3ONocKv0sZLnAy_4130_assertion SIO_000772 15869605 NP373201.RAnN0URdTS_8qq-T1pXSqb2sHHaDx3ONocKv0sZLnAy_4130_provenance.
- NP373201.RAnN0URdTS_8qq-T1pXSqb2sHHaDx3ONocKv0sZLnAy_4130_assertion wasDerivedFrom befree-20140225 NP373201.RAnN0URdTS_8qq-T1pXSqb2sHHaDx3ONocKv0sZLnAy_4130_provenance.
- NP373201.RAnN0URdTS_8qq-T1pXSqb2sHHaDx3ONocKv0sZLnAy_4130_assertion wasGeneratedBy ECO_0000203 NP373201.RAnN0URdTS_8qq-T1pXSqb2sHHaDx3ONocKv0sZLnAy_4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP373201.RAnN0URdTS_8qq-T1pXSqb2sHHaDx3ONocKv0sZLnAy_4130_provenance.