Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP119778.RAcOfikCEZgPEfgo-vEp2gfgdoNb94FeEXNWE3zx8iIyg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP119778.RAcOfikCEZgPEfgo-vEp2gfgdoNb94FeEXNWE3zx8iIyg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP119778.RAcOfikCEZgPEfgo-vEp2gfgdoNb94FeEXNWE3zx8iIyg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP119778.RAcOfikCEZgPEfgo-vEp2gfgdoNb94FeEXNWE3zx8iIyg130_provenance.
- NP119778.RAcOfikCEZgPEfgo-vEp2gfgdoNb94FeEXNWE3zx8iIyg130_assertion description "[We did not identify other loss of function mutations in ABCA3 among patients with E292V that would account for their RDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP119778.RAcOfikCEZgPEfgo-vEp2gfgdoNb94FeEXNWE3zx8iIyg130_provenance.
- NP119778.RAcOfikCEZgPEfgo-vEp2gfgdoNb94FeEXNWE3zx8iIyg130_assertion evidence source_evidence_literature NP119778.RAcOfikCEZgPEfgo-vEp2gfgdoNb94FeEXNWE3zx8iIyg130_provenance.
- NP119778.RAcOfikCEZgPEfgo-vEp2gfgdoNb94FeEXNWE3zx8iIyg130_assertion SIO_000772 18317237 NP119778.RAcOfikCEZgPEfgo-vEp2gfgdoNb94FeEXNWE3zx8iIyg130_provenance.
- NP119778.RAcOfikCEZgPEfgo-vEp2gfgdoNb94FeEXNWE3zx8iIyg130_assertion wasDerivedFrom gad-20150221 NP119778.RAcOfikCEZgPEfgo-vEp2gfgdoNb94FeEXNWE3zx8iIyg130_provenance.
- NP119778.RAcOfikCEZgPEfgo-vEp2gfgdoNb94FeEXNWE3zx8iIyg130_assertion wasGeneratedBy ECO_0000203 NP119778.RAcOfikCEZgPEfgo-vEp2gfgdoNb94FeEXNWE3zx8iIyg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP119778.RAcOfikCEZgPEfgo-vEp2gfgdoNb94FeEXNWE3zx8iIyg130_provenance.