Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP489419.RAYvA-4wLQOfInTJlX-VPSxk8If5_Xb7yRGn8gnZbdBXw130_assertion> ?p ?o ?g. }
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- NP489419.RAYvA-4wLQOfInTJlX-VPSxk8If5_Xb7yRGn8gnZbdBXw130_assertion type Assertion NP489419.RAYvA-4wLQOfInTJlX-VPSxk8If5_Xb7yRGn8gnZbdBXw130_head.
- NP489419.RAYvA-4wLQOfInTJlX-VPSxk8If5_Xb7yRGn8gnZbdBXw130_assertion description "[Curiously, although the index patient inherited both Bernard Soulier syndrome and factor XI deficiency (FXI: C = 1.3%), he had mild bleeding symptoms restricted only to ecchymoses and petechiae.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP489419.RAYvA-4wLQOfInTJlX-VPSxk8If5_Xb7yRGn8gnZbdBXw130_provenance.
- NP489419.RAYvA-4wLQOfInTJlX-VPSxk8If5_Xb7yRGn8gnZbdBXw130_assertion evidence source_evidence_literature NP489419.RAYvA-4wLQOfInTJlX-VPSxk8If5_Xb7yRGn8gnZbdBXw130_provenance.
- NP489419.RAYvA-4wLQOfInTJlX-VPSxk8If5_Xb7yRGn8gnZbdBXw130_assertion SIO_000772 15823864 NP489419.RAYvA-4wLQOfInTJlX-VPSxk8If5_Xb7yRGn8gnZbdBXw130_provenance.
- NP489419.RAYvA-4wLQOfInTJlX-VPSxk8If5_Xb7yRGn8gnZbdBXw130_assertion wasDerivedFrom befree-2016 NP489419.RAYvA-4wLQOfInTJlX-VPSxk8If5_Xb7yRGn8gnZbdBXw130_provenance.
- NP489419.RAYvA-4wLQOfInTJlX-VPSxk8If5_Xb7yRGn8gnZbdBXw130_assertion wasGeneratedBy ECO_0000203 NP489419.RAYvA-4wLQOfInTJlX-VPSxk8If5_Xb7yRGn8gnZbdBXw130_provenance.