Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP743874.RAGPM_POSfxBTvu41-L0PDNBfu_gh_OiVQHBP3CVGqhqM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP743874.RAGPM_POSfxBTvu41-L0PDNBfu_gh_OiVQHBP3CVGqhqM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP743874.RAGPM_POSfxBTvu41-L0PDNBfu_gh_OiVQHBP3CVGqhqM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP743874.RAGPM_POSfxBTvu41-L0PDNBfu_gh_OiVQHBP3CVGqhqM130_provenance.
- NP743874.RAGPM_POSfxBTvu41-L0PDNBfu_gh_OiVQHBP3CVGqhqM130_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." NP743874.RAGPM_POSfxBTvu41-L0PDNBfu_gh_OiVQHBP3CVGqhqM130_provenance.
- NP743874.RAGPM_POSfxBTvu41-L0PDNBfu_gh_OiVQHBP3CVGqhqM130_assertion evidence source_evidence_literature NP743874.RAGPM_POSfxBTvu41-L0PDNBfu_gh_OiVQHBP3CVGqhqM130_provenance.
- NP743874.RAGPM_POSfxBTvu41-L0PDNBfu_gh_OiVQHBP3CVGqhqM130_assertion SIO_000772 19506355 NP743874.RAGPM_POSfxBTvu41-L0PDNBfu_gh_OiVQHBP3CVGqhqM130_provenance.
- NP743874.RAGPM_POSfxBTvu41-L0PDNBfu_gh_OiVQHBP3CVGqhqM130_assertion wasDerivedFrom befree-2016 NP743874.RAGPM_POSfxBTvu41-L0PDNBfu_gh_OiVQHBP3CVGqhqM130_provenance.
- NP743874.RAGPM_POSfxBTvu41-L0PDNBfu_gh_OiVQHBP3CVGqhqM130_assertion wasGeneratedBy ECO_0000203 NP743874.RAGPM_POSfxBTvu41-L0PDNBfu_gh_OiVQHBP3CVGqhqM130_provenance.
- befree-2016 importedOn "2016-02-19" NP743874.RAGPM_POSfxBTvu41-L0PDNBfu_gh_OiVQHBP3CVGqhqM130_provenance.