Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_assertion> ?p ?o ?g. }
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- NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_assertion type Assertion NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_head.
- NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_assertion description "[After confirming clinically suspected thromboembolism with suitable imaging methods, pediatric patients should be screened for common gene mutations (factor V G1691A, prothrombin G20210A and MTHFR C677T genotypes), rare genetic deficiencies (protein C, protein S, antithrombin, and plasminogen), and new candidates for genetic thrombophilia causing elevated levels of lipoprotein(a), and homocysteine, and probable genetic risk factors (elevations in fibrinogen, factor IX, and factor VIIIC, and decreases in factor XII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_provenance.
- NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_assertion evidence source_evidence_literature NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_provenance.
- NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_assertion SIO_000772 12172465 NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_provenance.
- NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_assertion wasDerivedFrom befree-20150227 NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_provenance.
- NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_assertion wasGeneratedBy ECO_0000203 NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_provenance.