Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP708538.RAABcgSZD3U_7y2Nxl4HVfNbFZNDzCmqUESFY2dwXMDoE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP708538.RAABcgSZD3U_7y2Nxl4HVfNbFZNDzCmqUESFY2dwXMDoE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP708538.RAABcgSZD3U_7y2Nxl4HVfNbFZNDzCmqUESFY2dwXMDoE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP708538.RAABcgSZD3U_7y2Nxl4HVfNbFZNDzCmqUESFY2dwXMDoE130_provenance.
- NP708538.RAABcgSZD3U_7y2Nxl4HVfNbFZNDzCmqUESFY2dwXMDoE130_assertion description "[Interestingly, genetic screening of patients with dilated cardiomyopathy and congenital heart disease has revealed TBX20 variants in three sporadic and two familial cases that were not found in controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708538.RAABcgSZD3U_7y2Nxl4HVfNbFZNDzCmqUESFY2dwXMDoE130_provenance.
- NP708538.RAABcgSZD3U_7y2Nxl4HVfNbFZNDzCmqUESFY2dwXMDoE130_assertion evidence source_evidence_literature NP708538.RAABcgSZD3U_7y2Nxl4HVfNbFZNDzCmqUESFY2dwXMDoE130_provenance.
- NP708538.RAABcgSZD3U_7y2Nxl4HVfNbFZNDzCmqUESFY2dwXMDoE130_assertion SIO_000772 19074289 NP708538.RAABcgSZD3U_7y2Nxl4HVfNbFZNDzCmqUESFY2dwXMDoE130_provenance.
- NP708538.RAABcgSZD3U_7y2Nxl4HVfNbFZNDzCmqUESFY2dwXMDoE130_assertion wasDerivedFrom befree-2016 NP708538.RAABcgSZD3U_7y2Nxl4HVfNbFZNDzCmqUESFY2dwXMDoE130_provenance.
- NP708538.RAABcgSZD3U_7y2Nxl4HVfNbFZNDzCmqUESFY2dwXMDoE130_assertion wasGeneratedBy ECO_0000203 NP708538.RAABcgSZD3U_7y2Nxl4HVfNbFZNDzCmqUESFY2dwXMDoE130_provenance.
- befree-2016 importedOn "2016-02-19" NP708538.RAABcgSZD3U_7y2Nxl4HVfNbFZNDzCmqUESFY2dwXMDoE130_provenance.