Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP930444.RAxsD1Bxg_HWX8usZr6C_CowxPxETWSGnamM3qhlOFfxU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP930444.RAxsD1Bxg_HWX8usZr6C_CowxPxETWSGnamM3qhlOFfxU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP930444.RAxsD1Bxg_HWX8usZr6C_CowxPxETWSGnamM3qhlOFfxU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP930444.RAxsD1Bxg_HWX8usZr6C_CowxPxETWSGnamM3qhlOFfxU130_provenance.
- NP930444.RAxsD1Bxg_HWX8usZr6C_CowxPxETWSGnamM3qhlOFfxU130_assertion description "[In addition, the tail regions of A-type lamin variants that occur in Dunnigan-type familial partial lipodystrophy of (R482W) and Hutchison Gilford progeria syndrome (?607-656) bind to the SREBP1 polypeptide in vitro, and the corresponding FLAG-tagged full-length lamin variants co-immunoprecipitate the SREBP1 polypeptide in cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP930444.RAxsD1Bxg_HWX8usZr6C_CowxPxETWSGnamM3qhlOFfxU130_provenance.
- NP930444.RAxsD1Bxg_HWX8usZr6C_CowxPxETWSGnamM3qhlOFfxU130_assertion evidence source_evidence_literature NP930444.RAxsD1Bxg_HWX8usZr6C_CowxPxETWSGnamM3qhlOFfxU130_provenance.
- NP930444.RAxsD1Bxg_HWX8usZr6C_CowxPxETWSGnamM3qhlOFfxU130_assertion SIO_000772 21993218 NP930444.RAxsD1Bxg_HWX8usZr6C_CowxPxETWSGnamM3qhlOFfxU130_provenance.
- NP930444.RAxsD1Bxg_HWX8usZr6C_CowxPxETWSGnamM3qhlOFfxU130_assertion wasDerivedFrom befree-2016 NP930444.RAxsD1Bxg_HWX8usZr6C_CowxPxETWSGnamM3qhlOFfxU130_provenance.
- NP930444.RAxsD1Bxg_HWX8usZr6C_CowxPxETWSGnamM3qhlOFfxU130_assertion wasGeneratedBy ECO_0000203 NP930444.RAxsD1Bxg_HWX8usZr6C_CowxPxETWSGnamM3qhlOFfxU130_provenance.
- befree-2016 importedOn "2016-02-19" NP930444.RAxsD1Bxg_HWX8usZr6C_CowxPxETWSGnamM3qhlOFfxU130_provenance.