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- source_evidence_literature type ECO_0000212 NP867517.RA_AWuEGGaYsvzCzmfvQlFqDp5G4ZIq-yMUDmorZSlBNw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867517.RA_AWuEGGaYsvzCzmfvQlFqDp5G4ZIq-yMUDmorZSlBNw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867517.RA_AWuEGGaYsvzCzmfvQlFqDp5G4ZIq-yMUDmorZSlBNw130_provenance.
- NP867517.RA_AWuEGGaYsvzCzmfvQlFqDp5G4ZIq-yMUDmorZSlBNw130_assertion description "[It was the aim of the present study to prospectively evaluate clinical events of 60 heterozygous patients with VWD Vicenza (VWD-VI) carrying R1205H VWF mutation and 23 with C1130F mutation, both characterised by markedly increased VWF clearance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867517.RA_AWuEGGaYsvzCzmfvQlFqDp5G4ZIq-yMUDmorZSlBNw130_provenance.
- NP867517.RA_AWuEGGaYsvzCzmfvQlFqDp5G4ZIq-yMUDmorZSlBNw130_assertion evidence source_evidence_literature NP867517.RA_AWuEGGaYsvzCzmfvQlFqDp5G4ZIq-yMUDmorZSlBNw130_provenance.
- NP867517.RA_AWuEGGaYsvzCzmfvQlFqDp5G4ZIq-yMUDmorZSlBNw130_assertion SIO_000772 21264446 NP867517.RA_AWuEGGaYsvzCzmfvQlFqDp5G4ZIq-yMUDmorZSlBNw130_provenance.
- NP867517.RA_AWuEGGaYsvzCzmfvQlFqDp5G4ZIq-yMUDmorZSlBNw130_assertion wasDerivedFrom befree-2016 NP867517.RA_AWuEGGaYsvzCzmfvQlFqDp5G4ZIq-yMUDmorZSlBNw130_provenance.
- NP867517.RA_AWuEGGaYsvzCzmfvQlFqDp5G4ZIq-yMUDmorZSlBNw130_assertion wasGeneratedBy ECO_0000203 NP867517.RA_AWuEGGaYsvzCzmfvQlFqDp5G4ZIq-yMUDmorZSlBNw130_provenance.
- befree-2016 importedOn "2016-02-19" NP867517.RA_AWuEGGaYsvzCzmfvQlFqDp5G4ZIq-yMUDmorZSlBNw130_provenance.