Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1327435.RAD-yyFnXnWvsgEv_erEPlB0DpUjy1Q8TYHJAeQJec210130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1327435.RAD-yyFnXnWvsgEv_erEPlB0DpUjy1Q8TYHJAeQJec210130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1327435.RAD-yyFnXnWvsgEv_erEPlB0DpUjy1Q8TYHJAeQJec210130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1327435.RAD-yyFnXnWvsgEv_erEPlB0DpUjy1Q8TYHJAeQJec210130_provenance.
- NP1327435.RAD-yyFnXnWvsgEv_erEPlB0DpUjy1Q8TYHJAeQJec210130_assertion description "[The Kell blood group examination on erythrocytes disclosed that the propositus had McLeod phenotype, and his mother and one of his sisters were carriers of the McLeod phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327435.RAD-yyFnXnWvsgEv_erEPlB0DpUjy1Q8TYHJAeQJec210130_provenance.
- NP1327435.RAD-yyFnXnWvsgEv_erEPlB0DpUjy1Q8TYHJAeQJec210130_assertion evidence source_evidence_literature NP1327435.RAD-yyFnXnWvsgEv_erEPlB0DpUjy1Q8TYHJAeQJec210130_provenance.
- NP1327435.RAD-yyFnXnWvsgEv_erEPlB0DpUjy1Q8TYHJAeQJec210130_assertion SIO_000772 7931422 NP1327435.RAD-yyFnXnWvsgEv_erEPlB0DpUjy1Q8TYHJAeQJec210130_provenance.
- NP1327435.RAD-yyFnXnWvsgEv_erEPlB0DpUjy1Q8TYHJAeQJec210130_assertion wasDerivedFrom befree-2016 NP1327435.RAD-yyFnXnWvsgEv_erEPlB0DpUjy1Q8TYHJAeQJec210130_provenance.
- NP1327435.RAD-yyFnXnWvsgEv_erEPlB0DpUjy1Q8TYHJAeQJec210130_assertion wasGeneratedBy ECO_0000203 NP1327435.RAD-yyFnXnWvsgEv_erEPlB0DpUjy1Q8TYHJAeQJec210130_provenance.
- befree-2016 importedOn "2016-02-19" NP1327435.RAD-yyFnXnWvsgEv_erEPlB0DpUjy1Q8TYHJAeQJec210130_provenance.