Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP731611.RA09D85xZWh1apYgiDEo4zNRTDg8zBVFlokTFFg1J8qLg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP731611.RA09D85xZWh1apYgiDEo4zNRTDg8zBVFlokTFFg1J8qLg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP731611.RA09D85xZWh1apYgiDEo4zNRTDg8zBVFlokTFFg1J8qLg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP731611.RA09D85xZWh1apYgiDEo4zNRTDg8zBVFlokTFFg1J8qLg130_provenance.
- NP731611.RA09D85xZWh1apYgiDEo4zNRTDg8zBVFlokTFFg1J8qLg130_assertion description "[These results provide important evidence that the mutation of CITED2 may play a role in the development of congenital heart disease (CHD) in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP731611.RA09D85xZWh1apYgiDEo4zNRTDg8zBVFlokTFFg1J8qLg130_provenance.
- NP731611.RA09D85xZWh1apYgiDEo4zNRTDg8zBVFlokTFFg1J8qLg130_assertion evidence source_evidence_literature NP731611.RA09D85xZWh1apYgiDEo4zNRTDg8zBVFlokTFFg1J8qLg130_provenance.
- NP731611.RA09D85xZWh1apYgiDEo4zNRTDg8zBVFlokTFFg1J8qLg130_assertion SIO_000772 22735262 NP731611.RA09D85xZWh1apYgiDEo4zNRTDg8zBVFlokTFFg1J8qLg130_provenance.
- NP731611.RA09D85xZWh1apYgiDEo4zNRTDg8zBVFlokTFFg1J8qLg130_assertion wasDerivedFrom befree-20140225 NP731611.RA09D85xZWh1apYgiDEo4zNRTDg8zBVFlokTFFg1J8qLg130_provenance.
- NP731611.RA09D85xZWh1apYgiDEo4zNRTDg8zBVFlokTFFg1J8qLg130_assertion wasGeneratedBy ECO_0000203 NP731611.RA09D85xZWh1apYgiDEo4zNRTDg8zBVFlokTFFg1J8qLg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP731611.RA09D85xZWh1apYgiDEo4zNRTDg8zBVFlokTFFg1J8qLg130_provenance.