Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_provenance.
- NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_assertion wasGeneratedBy ECO_0000218 NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_provenance.
- NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_assertion wasDerivedFrom uniprot-2016 NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_provenance.
- NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_assertion SIO_000772 8123843 NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_provenance.
- NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_assertion evidence source_evidence_curated NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_provenance.
- NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_assertion description "[Leu 697-->Val mutation in mature von Willebrand factor is responsible for type IIB von Willebrand disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_provenance.