Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP322729.RAQ79igHMr-XQEyEO3DEdQ8O91yvgStODGBBVAw14OuNo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP322729.RAQ79igHMr-XQEyEO3DEdQ8O91yvgStODGBBVAw14OuNo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP322729.RAQ79igHMr-XQEyEO3DEdQ8O91yvgStODGBBVAw14OuNo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP322729.RAQ79igHMr-XQEyEO3DEdQ8O91yvgStODGBBVAw14OuNo130_provenance.
- NP322729.RAQ79igHMr-XQEyEO3DEdQ8O91yvgStODGBBVAw14OuNo130_assertion description "[The effects of S185F are compared with those of two mutations in residues 175 and 180 of human alpha-tropomyosin 1 which cause familial hypertrophic cardiomyopathy (HCM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322729.RAQ79igHMr-XQEyEO3DEdQ8O91yvgStODGBBVAw14OuNo130_provenance.
- NP322729.RAQ79igHMr-XQEyEO3DEdQ8O91yvgStODGBBVAw14OuNo130_assertion evidence source_evidence_literature NP322729.RAQ79igHMr-XQEyEO3DEdQ8O91yvgStODGBBVAw14OuNo130_provenance.
- NP322729.RAQ79igHMr-XQEyEO3DEdQ8O91yvgStODGBBVAw14OuNo130_assertion SIO_000772 11359941 NP322729.RAQ79igHMr-XQEyEO3DEdQ8O91yvgStODGBBVAw14OuNo130_provenance.
- NP322729.RAQ79igHMr-XQEyEO3DEdQ8O91yvgStODGBBVAw14OuNo130_assertion wasDerivedFrom befree-20140225 NP322729.RAQ79igHMr-XQEyEO3DEdQ8O91yvgStODGBBVAw14OuNo130_provenance.
- NP322729.RAQ79igHMr-XQEyEO3DEdQ8O91yvgStODGBBVAw14OuNo130_assertion wasGeneratedBy ECO_0000203 NP322729.RAQ79igHMr-XQEyEO3DEdQ8O91yvgStODGBBVAw14OuNo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP322729.RAQ79igHMr-XQEyEO3DEdQ8O91yvgStODGBBVAw14OuNo130_provenance.