Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_provenance.
- 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.
- uniprot-2016 importedOn "2016-01-25" NP7609.RAdf3P1e5MARFsjAgtwoVyGW4-vi0RKvCp444ULJGrBWo130_provenance.