Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP585041.RAsrjQiJWdzAbXFuQG7Oj5yDC7ng1znTvXWecMvNoz5Yc130_assertion> ?p ?o ?g. }
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- NP585041.RAsrjQiJWdzAbXFuQG7Oj5yDC7ng1znTvXWecMvNoz5Yc130_assertion type Assertion NP585041.RAsrjQiJWdzAbXFuQG7Oj5yDC7ng1znTvXWecMvNoz5Yc130_head.
- NP585041.RAsrjQiJWdzAbXFuQG7Oj5yDC7ng1znTvXWecMvNoz5Yc130_assertion description "[To provide a complete database of mutations and polymorphisms associated with factor XI deficiency we collected all available data on hereditary factor XI deficiency from main biological and medical databases [http://ncbi.nlm.nih.gov/pubmed and http://ncbi.nlm.nih.gov/omim (OMIM reference 264900) and the Human Gene Mutation Database for F11 mutations http://uwcmml1s.uwcm.ac.uk/uwcm/mg/search/119891.html] as well as from contributions to international congresses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585041.RAsrjQiJWdzAbXFuQG7Oj5yDC7ng1znTvXWecMvNoz5Yc130_provenance.
- NP585041.RAsrjQiJWdzAbXFuQG7Oj5yDC7ng1znTvXWecMvNoz5Yc130_assertion evidence source_evidence_literature NP585041.RAsrjQiJWdzAbXFuQG7Oj5yDC7ng1znTvXWecMvNoz5Yc130_provenance.
- NP585041.RAsrjQiJWdzAbXFuQG7Oj5yDC7ng1znTvXWecMvNoz5Yc130_assertion SIO_000772 15870541 NP585041.RAsrjQiJWdzAbXFuQG7Oj5yDC7ng1znTvXWecMvNoz5Yc130_provenance.
- NP585041.RAsrjQiJWdzAbXFuQG7Oj5yDC7ng1znTvXWecMvNoz5Yc130_assertion wasDerivedFrom befree-20140225 NP585041.RAsrjQiJWdzAbXFuQG7Oj5yDC7ng1znTvXWecMvNoz5Yc130_provenance.
- NP585041.RAsrjQiJWdzAbXFuQG7Oj5yDC7ng1znTvXWecMvNoz5Yc130_assertion wasGeneratedBy ECO_0000203 NP585041.RAsrjQiJWdzAbXFuQG7Oj5yDC7ng1znTvXWecMvNoz5Yc130_provenance.