Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_assertion> ?p ?o ?g. }
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- NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_assertion type Assertion NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_head.
- NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_assertion description "[Type�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." NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_provenance.
- NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_assertion evidence source_evidence_curated NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_provenance.
- NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_assertion SIO_000772 23910795 NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_provenance.
- NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_assertion wasDerivedFrom uniprot-2016 NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_provenance.
- NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_assertion wasGeneratedBy ECO_0000218 NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_provenance.