Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP990995.RAdb1g2QBUurSEVk0V6-1RfV87866xqh1EppdzLXa3qpo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP990995.RAdb1g2QBUurSEVk0V6-1RfV87866xqh1EppdzLXa3qpo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP990995.RAdb1g2QBUurSEVk0V6-1RfV87866xqh1EppdzLXa3qpo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP990995.RAdb1g2QBUurSEVk0V6-1RfV87866xqh1EppdzLXa3qpo130_provenance.
- NP990995.RAdb1g2QBUurSEVk0V6-1RfV87866xqh1EppdzLXa3qpo130_assertion description "[The folliculin-FNIP1 pathway deleted in human Birt-Hogg-Dub� syndrome is required for murine B-cell development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990995.RAdb1g2QBUurSEVk0V6-1RfV87866xqh1EppdzLXa3qpo130_provenance.
- NP990995.RAdb1g2QBUurSEVk0V6-1RfV87866xqh1EppdzLXa3qpo130_assertion evidence source_evidence_literature NP990995.RAdb1g2QBUurSEVk0V6-1RfV87866xqh1EppdzLXa3qpo130_provenance.
- NP990995.RAdb1g2QBUurSEVk0V6-1RfV87866xqh1EppdzLXa3qpo130_assertion SIO_000772 22709692 NP990995.RAdb1g2QBUurSEVk0V6-1RfV87866xqh1EppdzLXa3qpo130_provenance.
- NP990995.RAdb1g2QBUurSEVk0V6-1RfV87866xqh1EppdzLXa3qpo130_assertion wasDerivedFrom befree-2016 NP990995.RAdb1g2QBUurSEVk0V6-1RfV87866xqh1EppdzLXa3qpo130_provenance.
- NP990995.RAdb1g2QBUurSEVk0V6-1RfV87866xqh1EppdzLXa3qpo130_assertion wasGeneratedBy ECO_0000203 NP990995.RAdb1g2QBUurSEVk0V6-1RfV87866xqh1EppdzLXa3qpo130_provenance.
- befree-2016 importedOn "2016-02-19" NP990995.RAdb1g2QBUurSEVk0V6-1RfV87866xqh1EppdzLXa3qpo130_provenance.