Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP534291.RA2VLOBD3S6lcfVTI_FiMJG9aRlUxLpDjndUKRLk_FBGY130_assertion> ?p ?o ?g. }
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- NP534291.RA2VLOBD3S6lcfVTI_FiMJG9aRlUxLpDjndUKRLk_FBGY130_assertion type Assertion NP534291.RA2VLOBD3S6lcfVTI_FiMJG9aRlUxLpDjndUKRLk_FBGY130_head.
- NP534291.RA2VLOBD3S6lcfVTI_FiMJG9aRlUxLpDjndUKRLk_FBGY130_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." NP534291.RA2VLOBD3S6lcfVTI_FiMJG9aRlUxLpDjndUKRLk_FBGY130_provenance.
- NP534291.RA2VLOBD3S6lcfVTI_FiMJG9aRlUxLpDjndUKRLk_FBGY130_assertion evidence source_evidence_literature NP534291.RA2VLOBD3S6lcfVTI_FiMJG9aRlUxLpDjndUKRLk_FBGY130_provenance.
- NP534291.RA2VLOBD3S6lcfVTI_FiMJG9aRlUxLpDjndUKRLk_FBGY130_assertion SIO_000772 15009458 NP534291.RA2VLOBD3S6lcfVTI_FiMJG9aRlUxLpDjndUKRLk_FBGY130_provenance.
- NP534291.RA2VLOBD3S6lcfVTI_FiMJG9aRlUxLpDjndUKRLk_FBGY130_assertion wasDerivedFrom befree-20140225 NP534291.RA2VLOBD3S6lcfVTI_FiMJG9aRlUxLpDjndUKRLk_FBGY130_provenance.
- NP534291.RA2VLOBD3S6lcfVTI_FiMJG9aRlUxLpDjndUKRLk_FBGY130_assertion wasGeneratedBy ECO_0000203 NP534291.RA2VLOBD3S6lcfVTI_FiMJG9aRlUxLpDjndUKRLk_FBGY130_provenance.