Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_provenance.
- 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.
- uniprot-20150221 importedOn "2015-02-21" NP762.RAIGtMANIjzpdcQvkd4HJLdEQC9rc5EzS4uFc8YinaTzU130_provenance.