Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP365239.RAy5wdpDCdQ8ylqyugDv86yrQcCy_AFLk8koriezhOdbs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP365239.RAy5wdpDCdQ8ylqyugDv86yrQcCy_AFLk8koriezhOdbs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP365239.RAy5wdpDCdQ8ylqyugDv86yrQcCy_AFLk8koriezhOdbs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP365239.RAy5wdpDCdQ8ylqyugDv86yrQcCy_AFLk8koriezhOdbs130_provenance.
- NP365239.RAy5wdpDCdQ8ylqyugDv86yrQcCy_AFLk8koriezhOdbs130_assertion description "[Novel EDNRB mutations have been detected in non-syndromic HD patients with heterozygous forms, and homozygous mutations of the EDNRB or the EDN3 genes have been reported in HD patients associated with type 2 Waardenburg syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP365239.RAy5wdpDCdQ8ylqyugDv86yrQcCy_AFLk8koriezhOdbs130_provenance.
- NP365239.RAy5wdpDCdQ8ylqyugDv86yrQcCy_AFLk8koriezhOdbs130_assertion evidence source_evidence_literature NP365239.RAy5wdpDCdQ8ylqyugDv86yrQcCy_AFLk8koriezhOdbs130_provenance.
- NP365239.RAy5wdpDCdQ8ylqyugDv86yrQcCy_AFLk8koriezhOdbs130_assertion SIO_000772 9035203 NP365239.RAy5wdpDCdQ8ylqyugDv86yrQcCy_AFLk8koriezhOdbs130_provenance.
- NP365239.RAy5wdpDCdQ8ylqyugDv86yrQcCy_AFLk8koriezhOdbs130_assertion wasDerivedFrom befree-20150227 NP365239.RAy5wdpDCdQ8ylqyugDv86yrQcCy_AFLk8koriezhOdbs130_provenance.
- NP365239.RAy5wdpDCdQ8ylqyugDv86yrQcCy_AFLk8koriezhOdbs130_assertion wasGeneratedBy ECO_0000203 NP365239.RAy5wdpDCdQ8ylqyugDv86yrQcCy_AFLk8koriezhOdbs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP365239.RAy5wdpDCdQ8ylqyugDv86yrQcCy_AFLk8koriezhOdbs130_provenance.