Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP280144.RATJN4V0oWnipG7DfXrdx3OBDHtgf7HKL_otSAl4Fawus130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP280144.RATJN4V0oWnipG7DfXrdx3OBDHtgf7HKL_otSAl4Fawus130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280144.RATJN4V0oWnipG7DfXrdx3OBDHtgf7HKL_otSAl4Fawus130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280144.RATJN4V0oWnipG7DfXrdx3OBDHtgf7HKL_otSAl4Fawus130_provenance.
- NP280144.RATJN4V0oWnipG7DfXrdx3OBDHtgf7HKL_otSAl4Fawus130_assertion description "[In this report we describe the further investigation of the von Willebrand factor (vWF)/FVIII interaction in a type 1 von Willebrand disease patient characterized by discrepant VIII:C levels as determined by one-stage and two-stage VIII:C assays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280144.RATJN4V0oWnipG7DfXrdx3OBDHtgf7HKL_otSAl4Fawus130_provenance.
- NP280144.RATJN4V0oWnipG7DfXrdx3OBDHtgf7HKL_otSAl4Fawus130_assertion evidence source_evidence_literature NP280144.RATJN4V0oWnipG7DfXrdx3OBDHtgf7HKL_otSAl4Fawus130_provenance.
- NP280144.RATJN4V0oWnipG7DfXrdx3OBDHtgf7HKL_otSAl4Fawus130_assertion SIO_000772 8562925 NP280144.RATJN4V0oWnipG7DfXrdx3OBDHtgf7HKL_otSAl4Fawus130_provenance.
- NP280144.RATJN4V0oWnipG7DfXrdx3OBDHtgf7HKL_otSAl4Fawus130_assertion wasDerivedFrom befree-20140225 NP280144.RATJN4V0oWnipG7DfXrdx3OBDHtgf7HKL_otSAl4Fawus130_provenance.
- NP280144.RATJN4V0oWnipG7DfXrdx3OBDHtgf7HKL_otSAl4Fawus130_assertion wasGeneratedBy ECO_0000203 NP280144.RATJN4V0oWnipG7DfXrdx3OBDHtgf7HKL_otSAl4Fawus130_provenance.
- befree-20140225 importedOn "2014-02-25" NP280144.RATJN4V0oWnipG7DfXrdx3OBDHtgf7HKL_otSAl4Fawus130_provenance.