Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_provenance.
- NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_assertion description "[von Willebrand disease (VWD) type 3 is a rare disorder characterized by absent or <0.1 UmL(-1) of ristocetin cofactor (VWF:RCo), and a very low level of factor VIII (FVIII:C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_provenance.
- NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_assertion evidence source_evidence_literature NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_provenance.
- NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_assertion SIO_000772 19563498 NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_provenance.
- NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_assertion wasDerivedFrom befree-20150227 NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_provenance.
- NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_assertion wasGeneratedBy ECO_0000203 NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_provenance.