Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP730127.RABBSskyz_trg7pRODGSorOpgthaRr4n_665dqayD_cds130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP730127.RABBSskyz_trg7pRODGSorOpgthaRr4n_665dqayD_cds130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP730127.RABBSskyz_trg7pRODGSorOpgthaRr4n_665dqayD_cds130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP730127.RABBSskyz_trg7pRODGSorOpgthaRr4n_665dqayD_cds130_provenance.
- NP730127.RABBSskyz_trg7pRODGSorOpgthaRr4n_665dqayD_cds130_assertion description "[The congenital or acquired deficiency of the von Willebrand factor (VWF) cleaving protease, ADAMTS-13 has been specifically associated with a diagnosis of thrombotic thrombocytopenic purpura (TTP), a microangiopathy characterized by the formation of occlusive platelet thrombi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP730127.RABBSskyz_trg7pRODGSorOpgthaRr4n_665dqayD_cds130_provenance.
- NP730127.RABBSskyz_trg7pRODGSorOpgthaRr4n_665dqayD_cds130_assertion evidence source_evidence_literature NP730127.RABBSskyz_trg7pRODGSorOpgthaRr4n_665dqayD_cds130_provenance.
- NP730127.RABBSskyz_trg7pRODGSorOpgthaRr4n_665dqayD_cds130_assertion SIO_000772 15521921 NP730127.RABBSskyz_trg7pRODGSorOpgthaRr4n_665dqayD_cds130_provenance.
- NP730127.RABBSskyz_trg7pRODGSorOpgthaRr4n_665dqayD_cds130_assertion wasDerivedFrom befree-20140225 NP730127.RABBSskyz_trg7pRODGSorOpgthaRr4n_665dqayD_cds130_provenance.
- NP730127.RABBSskyz_trg7pRODGSorOpgthaRr4n_665dqayD_cds130_assertion wasGeneratedBy ECO_0000203 NP730127.RABBSskyz_trg7pRODGSorOpgthaRr4n_665dqayD_cds130_provenance.
- befree-20140225 importedOn "2014-02-25" NP730127.RABBSskyz_trg7pRODGSorOpgthaRr4n_665dqayD_cds130_provenance.