Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP606310.RA--Zaxq0seMx4GtkCTBHoa3hAC-6N2kWNGC79wAHn5Vg130_assertion> ?p ?o ?g. }
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- NP606310.RA--Zaxq0seMx4GtkCTBHoa3hAC-6N2kWNGC79wAHn5Vg130_assertion type Assertion NP606310.RA--Zaxq0seMx4GtkCTBHoa3hAC-6N2kWNGC79wAHn5Vg130_head.
- NP606310.RA--Zaxq0seMx4GtkCTBHoa3hAC-6N2kWNGC79wAHn5Vg130_assertion description "[The defective FVIII carrier function of von Willebrand factor (VWF) identifies type 2N von Willebrand disease (VWD), a variant with a pattern resembling hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606310.RA--Zaxq0seMx4GtkCTBHoa3hAC-6N2kWNGC79wAHn5Vg130_provenance.
- NP606310.RA--Zaxq0seMx4GtkCTBHoa3hAC-6N2kWNGC79wAHn5Vg130_assertion evidence source_evidence_literature NP606310.RA--Zaxq0seMx4GtkCTBHoa3hAC-6N2kWNGC79wAHn5Vg130_provenance.
- NP606310.RA--Zaxq0seMx4GtkCTBHoa3hAC-6N2kWNGC79wAHn5Vg130_assertion SIO_000772 17456630 NP606310.RA--Zaxq0seMx4GtkCTBHoa3hAC-6N2kWNGC79wAHn5Vg130_provenance.
- NP606310.RA--Zaxq0seMx4GtkCTBHoa3hAC-6N2kWNGC79wAHn5Vg130_assertion wasDerivedFrom befree-2016 NP606310.RA--Zaxq0seMx4GtkCTBHoa3hAC-6N2kWNGC79wAHn5Vg130_provenance.
- NP606310.RA--Zaxq0seMx4GtkCTBHoa3hAC-6N2kWNGC79wAHn5Vg130_assertion wasGeneratedBy ECO_0000203 NP606310.RA--Zaxq0seMx4GtkCTBHoa3hAC-6N2kWNGC79wAHn5Vg130_provenance.