Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP824808.RAcCoTpUia06JMIn9YvtSrbwkcMCKv2NtzzCRBsvC4chI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP824808.RAcCoTpUia06JMIn9YvtSrbwkcMCKv2NtzzCRBsvC4chI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824808.RAcCoTpUia06JMIn9YvtSrbwkcMCKv2NtzzCRBsvC4chI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824808.RAcCoTpUia06JMIn9YvtSrbwkcMCKv2NtzzCRBsvC4chI130_provenance.
- NP824808.RAcCoTpUia06JMIn9YvtSrbwkcMCKv2NtzzCRBsvC4chI130_assertion description "[Here, we report the identification of a founder mutation in the BBS2 gene as the cause for the increased incidence of this developmental disorder in the Hutterite population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824808.RAcCoTpUia06JMIn9YvtSrbwkcMCKv2NtzzCRBsvC4chI130_provenance.
- NP824808.RAcCoTpUia06JMIn9YvtSrbwkcMCKv2NtzzCRBsvC4chI130_assertion evidence source_evidence_literature NP824808.RAcCoTpUia06JMIn9YvtSrbwkcMCKv2NtzzCRBsvC4chI130_provenance.
- NP824808.RAcCoTpUia06JMIn9YvtSrbwkcMCKv2NtzzCRBsvC4chI130_assertion SIO_000772 20618352 NP824808.RAcCoTpUia06JMIn9YvtSrbwkcMCKv2NtzzCRBsvC4chI130_provenance.
- NP824808.RAcCoTpUia06JMIn9YvtSrbwkcMCKv2NtzzCRBsvC4chI130_assertion wasDerivedFrom befree-2016 NP824808.RAcCoTpUia06JMIn9YvtSrbwkcMCKv2NtzzCRBsvC4chI130_provenance.
- NP824808.RAcCoTpUia06JMIn9YvtSrbwkcMCKv2NtzzCRBsvC4chI130_assertion wasGeneratedBy ECO_0000203 NP824808.RAcCoTpUia06JMIn9YvtSrbwkcMCKv2NtzzCRBsvC4chI130_provenance.
- befree-2016 importedOn "2016-02-19" NP824808.RAcCoTpUia06JMIn9YvtSrbwkcMCKv2NtzzCRBsvC4chI130_provenance.