Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_provenance.
- NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_assertion description "[HRM analysis represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent HCM genes. Identification of more HCM mutations will provide new insights into genotype/phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_provenance.
- NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_assertion evidence source_evidence_literature NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_provenance.
- NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_assertion SIO_000772 20800588 NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_provenance.
- NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_assertion wasDerivedFrom gad-20150221 NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_provenance.
- NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_assertion wasGeneratedBy ECO_0000203 NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_provenance.
- gad-20150221 importedOn "2015-02-21" NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_provenance.