Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP253.RA6V7YicflMSUPsmVDp8h3tLRzXk4K-_dS9HkklKoTUZg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP253.RA6V7YicflMSUPsmVDp8h3tLRzXk4K-_dS9HkklKoTUZg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP253.RA6V7YicflMSUPsmVDp8h3tLRzXk4K-_dS9HkklKoTUZg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP253.RA6V7YicflMSUPsmVDp8h3tLRzXk4K-_dS9HkklKoTUZg130_provenance.
- NP253.RA6V7YicflMSUPsmVDp8h3tLRzXk4K-_dS9HkklKoTUZg130_assertion description "[In the definite M-D group, 50% carried an SGCE mutation and one single patient in the probable group (4%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253.RA6V7YicflMSUPsmVDp8h3tLRzXk4K-_dS9HkklKoTUZg130_provenance.
- NP253.RA6V7YicflMSUPsmVDp8h3tLRzXk4K-_dS9HkklKoTUZg130_assertion evidence source_evidence_curated NP253.RA6V7YicflMSUPsmVDp8h3tLRzXk4K-_dS9HkklKoTUZg130_provenance.
- NP253.RA6V7YicflMSUPsmVDp8h3tLRzXk4K-_dS9HkklKoTUZg130_assertion SIO_000772 19066193 NP253.RA6V7YicflMSUPsmVDp8h3tLRzXk4K-_dS9HkklKoTUZg130_provenance.
- NP253.RA6V7YicflMSUPsmVDp8h3tLRzXk4K-_dS9HkklKoTUZg130_assertion wasDerivedFrom uniprot-20150221 NP253.RA6V7YicflMSUPsmVDp8h3tLRzXk4K-_dS9HkklKoTUZg130_provenance.
- NP253.RA6V7YicflMSUPsmVDp8h3tLRzXk4K-_dS9HkklKoTUZg130_assertion wasGeneratedBy ECO_0000218 NP253.RA6V7YicflMSUPsmVDp8h3tLRzXk4K-_dS9HkklKoTUZg130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP253.RA6V7YicflMSUPsmVDp8h3tLRzXk4K-_dS9HkklKoTUZg130_provenance.