Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP838176.RAD1MYITwKIbQ60fWIkvVoB0odmnY8_DH6V6CJilmhNxo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP838176.RAD1MYITwKIbQ60fWIkvVoB0odmnY8_DH6V6CJilmhNxo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP838176.RAD1MYITwKIbQ60fWIkvVoB0odmnY8_DH6V6CJilmhNxo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP838176.RAD1MYITwKIbQ60fWIkvVoB0odmnY8_DH6V6CJilmhNxo130_provenance.
- NP838176.RAD1MYITwKIbQ60fWIkvVoB0odmnY8_DH6V6CJilmhNxo130_assertion description "[We have developed a mouse model that mimics these features of CGL: the syndrome occurs in transgenic mice expressing a truncated version of a nuclear protein known as nSREBP-1c (for sterol-regulatory-element-binding protein-1c) under the control of the adipose-specific aP2 enhancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838176.RAD1MYITwKIbQ60fWIkvVoB0odmnY8_DH6V6CJilmhNxo130_provenance.
- NP838176.RAD1MYITwKIbQ60fWIkvVoB0odmnY8_DH6V6CJilmhNxo130_assertion evidence source_evidence_literature NP838176.RAD1MYITwKIbQ60fWIkvVoB0odmnY8_DH6V6CJilmhNxo130_provenance.
- NP838176.RAD1MYITwKIbQ60fWIkvVoB0odmnY8_DH6V6CJilmhNxo130_assertion SIO_000772 10485707 NP838176.RAD1MYITwKIbQ60fWIkvVoB0odmnY8_DH6V6CJilmhNxo130_provenance.
- NP838176.RAD1MYITwKIbQ60fWIkvVoB0odmnY8_DH6V6CJilmhNxo130_assertion wasDerivedFrom befree-20140225 NP838176.RAD1MYITwKIbQ60fWIkvVoB0odmnY8_DH6V6CJilmhNxo130_provenance.
- NP838176.RAD1MYITwKIbQ60fWIkvVoB0odmnY8_DH6V6CJilmhNxo130_assertion wasGeneratedBy ECO_0000203 NP838176.RAD1MYITwKIbQ60fWIkvVoB0odmnY8_DH6V6CJilmhNxo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP838176.RAD1MYITwKIbQ60fWIkvVoB0odmnY8_DH6V6CJilmhNxo130_provenance.