Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP743871.RAsN694ZG9T5e3q50XrrsO9SNtql9inWbxfdPb9OIGf4g130_provenance.