Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP417714.RANISWVwvDUVPHtl3bAbcYUpre_V_-gQRWRuiGfaH1soY130_assertion> ?p ?o ?g. }
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- NP417714.RANISWVwvDUVPHtl3bAbcYUpre_V_-gQRWRuiGfaH1soY130_assertion type Assertion NP417714.RANISWVwvDUVPHtl3bAbcYUpre_V_-gQRWRuiGfaH1soY130_head.
- NP417714.RANISWVwvDUVPHtl3bAbcYUpre_V_-gQRWRuiGfaH1soY130_assertion description "[ADAMTS13 severe enzymatic deficiency and mutations have been described in the congenital thrombotic thrombocytopenic purpura (TTP or Upshaw-Schulman syndrome), a rare and severe disease related to multivisceral microvascular thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417714.RANISWVwvDUVPHtl3bAbcYUpre_V_-gQRWRuiGfaH1soY130_provenance.
- NP417714.RANISWVwvDUVPHtl3bAbcYUpre_V_-gQRWRuiGfaH1soY130_assertion evidence source_evidence_literature NP417714.RANISWVwvDUVPHtl3bAbcYUpre_V_-gQRWRuiGfaH1soY130_provenance.
- NP417714.RANISWVwvDUVPHtl3bAbcYUpre_V_-gQRWRuiGfaH1soY130_assertion SIO_000772 15009458 NP417714.RANISWVwvDUVPHtl3bAbcYUpre_V_-gQRWRuiGfaH1soY130_provenance.
- NP417714.RANISWVwvDUVPHtl3bAbcYUpre_V_-gQRWRuiGfaH1soY130_assertion wasDerivedFrom befree-20140225 NP417714.RANISWVwvDUVPHtl3bAbcYUpre_V_-gQRWRuiGfaH1soY130_provenance.
- NP417714.RANISWVwvDUVPHtl3bAbcYUpre_V_-gQRWRuiGfaH1soY130_assertion wasGeneratedBy ECO_0000203 NP417714.RANISWVwvDUVPHtl3bAbcYUpre_V_-gQRWRuiGfaH1soY130_provenance.