Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP712518.RA7Fi5wWYAMDeiRe13AaFFXi-EncjF99-peWdSKCkZKBo130_assertion> ?p ?o ?g. }
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- NP712518.RA7Fi5wWYAMDeiRe13AaFFXi-EncjF99-peWdSKCkZKBo130_assertion type Assertion NP712518.RA7Fi5wWYAMDeiRe13AaFFXi-EncjF99-peWdSKCkZKBo130_head.
- NP712518.RA7Fi5wWYAMDeiRe13AaFFXi-EncjF99-peWdSKCkZKBo130_assertion description "[Nine patients belonging to this kindred underwent coagulation study for hereditary thrombophilia, which included plasminogen antigen and activity assays, an activated protein C resistance test, and genetic analysis for factor V Leiden mutation and for prothrombin variant 20210A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP712518.RA7Fi5wWYAMDeiRe13AaFFXi-EncjF99-peWdSKCkZKBo130_provenance.
- NP712518.RA7Fi5wWYAMDeiRe13AaFFXi-EncjF99-peWdSKCkZKBo130_assertion evidence source_evidence_literature NP712518.RA7Fi5wWYAMDeiRe13AaFFXi-EncjF99-peWdSKCkZKBo130_provenance.
- NP712518.RA7Fi5wWYAMDeiRe13AaFFXi-EncjF99-peWdSKCkZKBo130_assertion SIO_000772 10726047 NP712518.RA7Fi5wWYAMDeiRe13AaFFXi-EncjF99-peWdSKCkZKBo130_provenance.
- NP712518.RA7Fi5wWYAMDeiRe13AaFFXi-EncjF99-peWdSKCkZKBo130_assertion wasDerivedFrom befree-20140225 NP712518.RA7Fi5wWYAMDeiRe13AaFFXi-EncjF99-peWdSKCkZKBo130_provenance.
- NP712518.RA7Fi5wWYAMDeiRe13AaFFXi-EncjF99-peWdSKCkZKBo130_assertion wasGeneratedBy ECO_0000203 NP712518.RA7Fi5wWYAMDeiRe13AaFFXi-EncjF99-peWdSKCkZKBo130_provenance.