Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP499910.RAcCVqWC1b5p99lLPphdbp9QJ80BU5DT22cF1iof14cm4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP499910.RAcCVqWC1b5p99lLPphdbp9QJ80BU5DT22cF1iof14cm4130_assertion type Assertion NP499910.RAcCVqWC1b5p99lLPphdbp9QJ80BU5DT22cF1iof14cm4130_head.
- NP499910.RAcCVqWC1b5p99lLPphdbp9QJ80BU5DT22cF1iof14cm4130_assertion description "[As this is a third independent case of protein C Tochigi with thromboembolism, the mutation of Arg169 (CGG) to Trp169 (TGG) in the protein C gene may be a hot spot and a common type of genetic lesion in congenital protein C deficiency with thromboembolic complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499910.RAcCVqWC1b5p99lLPphdbp9QJ80BU5DT22cF1iof14cm4130_provenance.
- NP499910.RAcCVqWC1b5p99lLPphdbp9QJ80BU5DT22cF1iof14cm4130_assertion evidence source_evidence_literature NP499910.RAcCVqWC1b5p99lLPphdbp9QJ80BU5DT22cF1iof14cm4130_provenance.
- NP499910.RAcCVqWC1b5p99lLPphdbp9QJ80BU5DT22cF1iof14cm4130_assertion SIO_000772 1596024 NP499910.RAcCVqWC1b5p99lLPphdbp9QJ80BU5DT22cF1iof14cm4130_provenance.
- NP499910.RAcCVqWC1b5p99lLPphdbp9QJ80BU5DT22cF1iof14cm4130_assertion wasDerivedFrom befree-2016 NP499910.RAcCVqWC1b5p99lLPphdbp9QJ80BU5DT22cF1iof14cm4130_provenance.
- NP499910.RAcCVqWC1b5p99lLPphdbp9QJ80BU5DT22cF1iof14cm4130_assertion wasGeneratedBy ECO_0000203 NP499910.RAcCVqWC1b5p99lLPphdbp9QJ80BU5DT22cF1iof14cm4130_provenance.