Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP715303.RA_kRKtwkE0GZiMEmp4O4ER1o1FXC9XBpVqrToUT6oX24130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP715303.RA_kRKtwkE0GZiMEmp4O4ER1o1FXC9XBpVqrToUT6oX24130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715303.RA_kRKtwkE0GZiMEmp4O4ER1o1FXC9XBpVqrToUT6oX24130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715303.RA_kRKtwkE0GZiMEmp4O4ER1o1FXC9XBpVqrToUT6oX24130_provenance.
- NP715303.RA_kRKtwkE0GZiMEmp4O4ER1o1FXC9XBpVqrToUT6oX24130_assertion description "[MYH9 risk variants appear to be associated with primary FSGS with secondary hypertension, although nephrosclerosis may develop in response to hypertension in subjects homozygous for the MYH9 E1 risk haplotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715303.RA_kRKtwkE0GZiMEmp4O4ER1o1FXC9XBpVqrToUT6oX24130_provenance.
- NP715303.RA_kRKtwkE0GZiMEmp4O4ER1o1FXC9XBpVqrToUT6oX24130_assertion evidence source_evidence_literature NP715303.RA_kRKtwkE0GZiMEmp4O4ER1o1FXC9XBpVqrToUT6oX24130_provenance.
- NP715303.RA_kRKtwkE0GZiMEmp4O4ER1o1FXC9XBpVqrToUT6oX24130_assertion SIO_000772 19153477 NP715303.RA_kRKtwkE0GZiMEmp4O4ER1o1FXC9XBpVqrToUT6oX24130_provenance.
- NP715303.RA_kRKtwkE0GZiMEmp4O4ER1o1FXC9XBpVqrToUT6oX24130_assertion wasDerivedFrom befree-2016 NP715303.RA_kRKtwkE0GZiMEmp4O4ER1o1FXC9XBpVqrToUT6oX24130_provenance.
- NP715303.RA_kRKtwkE0GZiMEmp4O4ER1o1FXC9XBpVqrToUT6oX24130_assertion wasGeneratedBy ECO_0000203 NP715303.RA_kRKtwkE0GZiMEmp4O4ER1o1FXC9XBpVqrToUT6oX24130_provenance.
- befree-2016 importedOn "2016-02-19" NP715303.RA_kRKtwkE0GZiMEmp4O4ER1o1FXC9XBpVqrToUT6oX24130_provenance.