Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_assertion> ?p ?o ?g. }
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- NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_assertion type Assertion NP8757.RAB985qpevljc0jWAvOZ9ESDuWkjTGrQSGmcrO21dGpdQ130_head.
- 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.