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- source_evidence_literature type ECO_0000212 NP930447.RAjkeLPwc5L-_mfydhb0w_RhQvlnwo8MAUtW7ujB6whIU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP930447.RAjkeLPwc5L-_mfydhb0w_RhQvlnwo8MAUtW7ujB6whIU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP930447.RAjkeLPwc5L-_mfydhb0w_RhQvlnwo8MAUtW7ujB6whIU130_provenance.
- NP930447.RAjkeLPwc5L-_mfydhb0w_RhQvlnwo8MAUtW7ujB6whIU130_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." NP930447.RAjkeLPwc5L-_mfydhb0w_RhQvlnwo8MAUtW7ujB6whIU130_provenance.
- NP930447.RAjkeLPwc5L-_mfydhb0w_RhQvlnwo8MAUtW7ujB6whIU130_assertion evidence source_evidence_literature NP930447.RAjkeLPwc5L-_mfydhb0w_RhQvlnwo8MAUtW7ujB6whIU130_provenance.
- NP930447.RAjkeLPwc5L-_mfydhb0w_RhQvlnwo8MAUtW7ujB6whIU130_assertion SIO_000772 21993218 NP930447.RAjkeLPwc5L-_mfydhb0w_RhQvlnwo8MAUtW7ujB6whIU130_provenance.
- NP930447.RAjkeLPwc5L-_mfydhb0w_RhQvlnwo8MAUtW7ujB6whIU130_assertion wasDerivedFrom befree-2016 NP930447.RAjkeLPwc5L-_mfydhb0w_RhQvlnwo8MAUtW7ujB6whIU130_provenance.
- NP930447.RAjkeLPwc5L-_mfydhb0w_RhQvlnwo8MAUtW7ujB6whIU130_assertion wasGeneratedBy ECO_0000203 NP930447.RAjkeLPwc5L-_mfydhb0w_RhQvlnwo8MAUtW7ujB6whIU130_provenance.
- befree-2016 importedOn "2016-02-19" NP930447.RAjkeLPwc5L-_mfydhb0w_RhQvlnwo8MAUtW7ujB6whIU130_provenance.