Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418662.RAaeELnLcP5iwUOqTWxQTUMFbqhhUrbTmApohFBGsGyZM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418662.RAaeELnLcP5iwUOqTWxQTUMFbqhhUrbTmApohFBGsGyZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418662.RAaeELnLcP5iwUOqTWxQTUMFbqhhUrbTmApohFBGsGyZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418662.RAaeELnLcP5iwUOqTWxQTUMFbqhhUrbTmApohFBGsGyZM130_provenance.
- NP418662.RAaeELnLcP5iwUOqTWxQTUMFbqhhUrbTmApohFBGsGyZM130_assertion description "[With the assistance of improved base stacking hybridization, a low-density microarray, containing 12 capture probes, was used to identify 7 known hypertrophic cardiomyopathy-related mutations in the gene of MYH7 (beta-myosia heavy chain).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418662.RAaeELnLcP5iwUOqTWxQTUMFbqhhUrbTmApohFBGsGyZM130_provenance.
- NP418662.RAaeELnLcP5iwUOqTWxQTUMFbqhhUrbTmApohFBGsGyZM130_assertion evidence source_evidence_literature NP418662.RAaeELnLcP5iwUOqTWxQTUMFbqhhUrbTmApohFBGsGyZM130_provenance.
- NP418662.RAaeELnLcP5iwUOqTWxQTUMFbqhhUrbTmApohFBGsGyZM130_assertion SIO_000772 14584916 NP418662.RAaeELnLcP5iwUOqTWxQTUMFbqhhUrbTmApohFBGsGyZM130_provenance.
- NP418662.RAaeELnLcP5iwUOqTWxQTUMFbqhhUrbTmApohFBGsGyZM130_assertion wasDerivedFrom befree-2016 NP418662.RAaeELnLcP5iwUOqTWxQTUMFbqhhUrbTmApohFBGsGyZM130_provenance.
- NP418662.RAaeELnLcP5iwUOqTWxQTUMFbqhhUrbTmApohFBGsGyZM130_assertion wasGeneratedBy ECO_0000203 NP418662.RAaeELnLcP5iwUOqTWxQTUMFbqhhUrbTmApohFBGsGyZM130_provenance.
- befree-2016 importedOn "2016-02-19" NP418662.RAaeELnLcP5iwUOqTWxQTUMFbqhhUrbTmApohFBGsGyZM130_provenance.