Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_assertion> ?p ?o ?g. }
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- NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_assertion type Assertion NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_head.
- NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_assertion description "[TypeA II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_provenance.
- NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_assertion evidence source_evidence_curated NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_provenance.
- NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_assertion SIO_000772 23910795 NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_provenance.
- NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_assertion wasDerivedFrom uniprot-20150221 NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_provenance.
- NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_assertion wasGeneratedBy ECO_0000218 NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_provenance.