Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP50519.RA3N3OyWyt2sfw6HRKMsw_d6npPOKErfN10CBkvxZvm0M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP50519.RA3N3OyWyt2sfw6HRKMsw_d6npPOKErfN10CBkvxZvm0M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP50519.RA3N3OyWyt2sfw6HRKMsw_d6npPOKErfN10CBkvxZvm0M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP50519.RA3N3OyWyt2sfw6HRKMsw_d6npPOKErfN10CBkvxZvm0M130_provenance.
- NP50519.RA3N3OyWyt2sfw6HRKMsw_d6npPOKErfN10CBkvxZvm0M130_assertion description "[our data suggested that CYP1B1 germ line-inactivating mutations might increase the incidence of HCA in women with HNF1alpha mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50519.RA3N3OyWyt2sfw6HRKMsw_d6npPOKErfN10CBkvxZvm0M130_provenance.
- NP50519.RA3N3OyWyt2sfw6HRKMsw_d6npPOKErfN10CBkvxZvm0M130_assertion evidence source_evidence_literature NP50519.RA3N3OyWyt2sfw6HRKMsw_d6npPOKErfN10CBkvxZvm0M130_provenance.
- NP50519.RA3N3OyWyt2sfw6HRKMsw_d6npPOKErfN10CBkvxZvm0M130_assertion SIO_000772 17363580 NP50519.RA3N3OyWyt2sfw6HRKMsw_d6npPOKErfN10CBkvxZvm0M130_provenance.
- NP50519.RA3N3OyWyt2sfw6HRKMsw_d6npPOKErfN10CBkvxZvm0M130_assertion wasDerivedFrom gad-20150221 NP50519.RA3N3OyWyt2sfw6HRKMsw_d6npPOKErfN10CBkvxZvm0M130_provenance.
- NP50519.RA3N3OyWyt2sfw6HRKMsw_d6npPOKErfN10CBkvxZvm0M130_assertion wasGeneratedBy ECO_0000203 NP50519.RA3N3OyWyt2sfw6HRKMsw_d6npPOKErfN10CBkvxZvm0M130_provenance.
- gad-20150221 importedOn "2015-02-21" NP50519.RA3N3OyWyt2sfw6HRKMsw_d6npPOKErfN10CBkvxZvm0M130_provenance.