Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP279271.RAj_Wgl2UVY-_ge3_q7GCAdheS3mvcQXcKpFS5NHaCu6M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP279271.RAj_Wgl2UVY-_ge3_q7GCAdheS3mvcQXcKpFS5NHaCu6M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP279271.RAj_Wgl2UVY-_ge3_q7GCAdheS3mvcQXcKpFS5NHaCu6M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP279271.RAj_Wgl2UVY-_ge3_q7GCAdheS3mvcQXcKpFS5NHaCu6M130_provenance.
- NP279271.RAj_Wgl2UVY-_ge3_q7GCAdheS3mvcQXcKpFS5NHaCu6M130_assertion description "[A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279271.RAj_Wgl2UVY-_ge3_q7GCAdheS3mvcQXcKpFS5NHaCu6M130_provenance.
- NP279271.RAj_Wgl2UVY-_ge3_q7GCAdheS3mvcQXcKpFS5NHaCu6M130_assertion evidence source_evidence_literature NP279271.RAj_Wgl2UVY-_ge3_q7GCAdheS3mvcQXcKpFS5NHaCu6M130_provenance.
- NP279271.RAj_Wgl2UVY-_ge3_q7GCAdheS3mvcQXcKpFS5NHaCu6M130_assertion SIO_000772 19429631 NP279271.RAj_Wgl2UVY-_ge3_q7GCAdheS3mvcQXcKpFS5NHaCu6M130_provenance.
- NP279271.RAj_Wgl2UVY-_ge3_q7GCAdheS3mvcQXcKpFS5NHaCu6M130_assertion wasDerivedFrom befree-20150227 NP279271.RAj_Wgl2UVY-_ge3_q7GCAdheS3mvcQXcKpFS5NHaCu6M130_provenance.
- NP279271.RAj_Wgl2UVY-_ge3_q7GCAdheS3mvcQXcKpFS5NHaCu6M130_assertion wasGeneratedBy ECO_0000203 NP279271.RAj_Wgl2UVY-_ge3_q7GCAdheS3mvcQXcKpFS5NHaCu6M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP279271.RAj_Wgl2UVY-_ge3_q7GCAdheS3mvcQXcKpFS5NHaCu6M130_provenance.