Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1130313.RAm1QtDo15IRot0CLNrIS1hIpUDXNJ13vA2TSJI8VipbQ130_assertion> ?p ?o ?g. }
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- NP1130313.RAm1QtDo15IRot0CLNrIS1hIpUDXNJ13vA2TSJI8VipbQ130_assertion type Assertion NP1130313.RAm1QtDo15IRot0CLNrIS1hIpUDXNJ13vA2TSJI8VipbQ130_head.
- NP1130313.RAm1QtDo15IRot0CLNrIS1hIpUDXNJ13vA2TSJI8VipbQ130_assertion description "[Complete plasminogen activator inhibitor type 1 (PAI-1) deficiency is an exceedingly rare autosomal recessive bleeding disorder previously identified and reported in a large Old Order Amish (OOA) kindred in Indiana [Fay et�al.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1130313.RAm1QtDo15IRot0CLNrIS1hIpUDXNJ13vA2TSJI8VipbQ130_provenance.
- NP1130313.RAm1QtDo15IRot0CLNrIS1hIpUDXNJ13vA2TSJI8VipbQ130_assertion evidence source_evidence_literature NP1130313.RAm1QtDo15IRot0CLNrIS1hIpUDXNJ13vA2TSJI8VipbQ130_provenance.
- NP1130313.RAm1QtDo15IRot0CLNrIS1hIpUDXNJ13vA2TSJI8VipbQ130_assertion SIO_000772 24261743 NP1130313.RAm1QtDo15IRot0CLNrIS1hIpUDXNJ13vA2TSJI8VipbQ130_provenance.
- NP1130313.RAm1QtDo15IRot0CLNrIS1hIpUDXNJ13vA2TSJI8VipbQ130_assertion wasDerivedFrom befree-2016 NP1130313.RAm1QtDo15IRot0CLNrIS1hIpUDXNJ13vA2TSJI8VipbQ130_provenance.
- NP1130313.RAm1QtDo15IRot0CLNrIS1hIpUDXNJ13vA2TSJI8VipbQ130_assertion wasGeneratedBy ECO_0000203 NP1130313.RAm1QtDo15IRot0CLNrIS1hIpUDXNJ13vA2TSJI8VipbQ130_provenance.