Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_assertion> ?p ?o ?g. }
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- NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_assertion type Assertion NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_head.
- NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_assertion description "[Factor VIII-von Willebrand factor binding defects in autosomal recessive von Willebrand disease type Normandy and in mild hemophilia A. New insights into factor VIII-von Willebrand factor interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_provenance.
- NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_assertion evidence source_evidence_literature NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_provenance.
- NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_assertion SIO_000772 19506355 NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_provenance.
- NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_assertion wasDerivedFrom befree-2016 NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_provenance.
- NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_assertion wasGeneratedBy ECO_0000203 NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_provenance.