Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP139961.RAQo3ZwU3ZVYH60t5mPNaBBDNP2R-LspIo7CaaQUWzMYQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP139961.RAQo3ZwU3ZVYH60t5mPNaBBDNP2R-LspIo7CaaQUWzMYQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP139961.RAQo3ZwU3ZVYH60t5mPNaBBDNP2R-LspIo7CaaQUWzMYQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP139961.RAQo3ZwU3ZVYH60t5mPNaBBDNP2R-LspIo7CaaQUWzMYQ130_provenance.
- NP139961.RAQo3ZwU3ZVYH60t5mPNaBBDNP2R-LspIo7CaaQUWzMYQ130_assertion description "[Investigation of somatic NKX2-5 mutations in congenital heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP139961.RAQo3ZwU3ZVYH60t5mPNaBBDNP2R-LspIo7CaaQUWzMYQ130_provenance.
- NP139961.RAQo3ZwU3ZVYH60t5mPNaBBDNP2R-LspIo7CaaQUWzMYQ130_assertion evidence source_evidence_literature NP139961.RAQo3ZwU3ZVYH60t5mPNaBBDNP2R-LspIo7CaaQUWzMYQ130_provenance.
- NP139961.RAQo3ZwU3ZVYH60t5mPNaBBDNP2R-LspIo7CaaQUWzMYQ130_assertion SIO_000772 19181906 NP139961.RAQo3ZwU3ZVYH60t5mPNaBBDNP2R-LspIo7CaaQUWzMYQ130_provenance.
- NP139961.RAQo3ZwU3ZVYH60t5mPNaBBDNP2R-LspIo7CaaQUWzMYQ130_assertion wasDerivedFrom gad-20150221 NP139961.RAQo3ZwU3ZVYH60t5mPNaBBDNP2R-LspIo7CaaQUWzMYQ130_provenance.
- NP139961.RAQo3ZwU3ZVYH60t5mPNaBBDNP2R-LspIo7CaaQUWzMYQ130_assertion wasGeneratedBy ECO_0000203 NP139961.RAQo3ZwU3ZVYH60t5mPNaBBDNP2R-LspIo7CaaQUWzMYQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP139961.RAQo3ZwU3ZVYH60t5mPNaBBDNP2R-LspIo7CaaQUWzMYQ130_provenance.