Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP184918.RANBTwmRI2naE1BYdF-frHxrR7izKCOnOwwYDkH0WC9yU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP184918.RANBTwmRI2naE1BYdF-frHxrR7izKCOnOwwYDkH0WC9yU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP184918.RANBTwmRI2naE1BYdF-frHxrR7izKCOnOwwYDkH0WC9yU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP184918.RANBTwmRI2naE1BYdF-frHxrR7izKCOnOwwYDkH0WC9yU130_provenance.
- NP184918.RANBTwmRI2naE1BYdF-frHxrR7izKCOnOwwYDkH0WC9yU130_assertion description "[Further studies are needed to explore contributions from other genetic factors such as rare variants in these genes and variation outside of these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184918.RANBTwmRI2naE1BYdF-frHxrR7izKCOnOwwYDkH0WC9yU130_provenance.
- NP184918.RANBTwmRI2naE1BYdF-frHxrR7izKCOnOwwYDkH0WC9yU130_assertion evidence source_evidence_literature NP184918.RANBTwmRI2naE1BYdF-frHxrR7izKCOnOwwYDkH0WC9yU130_provenance.
- NP184918.RANBTwmRI2naE1BYdF-frHxrR7izKCOnOwwYDkH0WC9yU130_assertion SIO_000772 20810604 NP184918.RANBTwmRI2naE1BYdF-frHxrR7izKCOnOwwYDkH0WC9yU130_provenance.
- NP184918.RANBTwmRI2naE1BYdF-frHxrR7izKCOnOwwYDkH0WC9yU130_assertion wasDerivedFrom gad-20150221 NP184918.RANBTwmRI2naE1BYdF-frHxrR7izKCOnOwwYDkH0WC9yU130_provenance.
- NP184918.RANBTwmRI2naE1BYdF-frHxrR7izKCOnOwwYDkH0WC9yU130_assertion wasGeneratedBy ECO_0000203 NP184918.RANBTwmRI2naE1BYdF-frHxrR7izKCOnOwwYDkH0WC9yU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP184918.RANBTwmRI2naE1BYdF-frHxrR7izKCOnOwwYDkH0WC9yU130_provenance.