Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1215301.RA1ec4fViODewQEwx86SZLGPsbTXFr0l58YS7XpeWQAQ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1215301.RA1ec4fViODewQEwx86SZLGPsbTXFr0l58YS7XpeWQAQ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1215301.RA1ec4fViODewQEwx86SZLGPsbTXFr0l58YS7XpeWQAQ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1215301.RA1ec4fViODewQEwx86SZLGPsbTXFr0l58YS7XpeWQAQ4130_provenance.
- NP1215301.RA1ec4fViODewQEwx86SZLGPsbTXFr0l58YS7XpeWQAQ4130_assertion description "[A targeted next-generation sequencing approach allowed the identification of a novel ACTN2 variant associated with midapical HCM and juvenile onset of atrial fibrillation, emphasizing the potential of such approach in HCM diagnostic screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215301.RA1ec4fViODewQEwx86SZLGPsbTXFr0l58YS7XpeWQAQ4130_provenance.
- NP1215301.RA1ec4fViODewQEwx86SZLGPsbTXFr0l58YS7XpeWQAQ4130_assertion evidence source_evidence_literature NP1215301.RA1ec4fViODewQEwx86SZLGPsbTXFr0l58YS7XpeWQAQ4130_provenance.
- NP1215301.RA1ec4fViODewQEwx86SZLGPsbTXFr0l58YS7XpeWQAQ4130_assertion SIO_000772 25173926 NP1215301.RA1ec4fViODewQEwx86SZLGPsbTXFr0l58YS7XpeWQAQ4130_provenance.
- NP1215301.RA1ec4fViODewQEwx86SZLGPsbTXFr0l58YS7XpeWQAQ4130_assertion wasDerivedFrom befree-2016 NP1215301.RA1ec4fViODewQEwx86SZLGPsbTXFr0l58YS7XpeWQAQ4130_provenance.
- NP1215301.RA1ec4fViODewQEwx86SZLGPsbTXFr0l58YS7XpeWQAQ4130_assertion wasGeneratedBy ECO_0000203 NP1215301.RA1ec4fViODewQEwx86SZLGPsbTXFr0l58YS7XpeWQAQ4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1215301.RA1ec4fViODewQEwx86SZLGPsbTXFr0l58YS7XpeWQAQ4130_provenance.