Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_assertion type Assertion NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_head.
- NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_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." NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_provenance.
- NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_assertion evidence source_evidence_literature NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_provenance.
- NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_assertion SIO_000772 17456630 NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_provenance.
- NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_assertion wasDerivedFrom befree-2016 NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_provenance.
- NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_assertion wasGeneratedBy ECO_0000203 NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_provenance.