Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP455009.RAGp0ULkWdc7KtMQvbde3UAdZMSN1oryMXt5_BcAcD_ew130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP455009.RAGp0ULkWdc7KtMQvbde3UAdZMSN1oryMXt5_BcAcD_ew130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP455009.RAGp0ULkWdc7KtMQvbde3UAdZMSN1oryMXt5_BcAcD_ew130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP455009.RAGp0ULkWdc7KtMQvbde3UAdZMSN1oryMXt5_BcAcD_ew130_provenance.
- NP455009.RAGp0ULkWdc7KtMQvbde3UAdZMSN1oryMXt5_BcAcD_ew130_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." NP455009.RAGp0ULkWdc7KtMQvbde3UAdZMSN1oryMXt5_BcAcD_ew130_provenance.
- NP455009.RAGp0ULkWdc7KtMQvbde3UAdZMSN1oryMXt5_BcAcD_ew130_assertion evidence source_evidence_literature NP455009.RAGp0ULkWdc7KtMQvbde3UAdZMSN1oryMXt5_BcAcD_ew130_provenance.
- NP455009.RAGp0ULkWdc7KtMQvbde3UAdZMSN1oryMXt5_BcAcD_ew130_assertion SIO_000772 21993218 NP455009.RAGp0ULkWdc7KtMQvbde3UAdZMSN1oryMXt5_BcAcD_ew130_provenance.
- NP455009.RAGp0ULkWdc7KtMQvbde3UAdZMSN1oryMXt5_BcAcD_ew130_assertion wasDerivedFrom befree-20140225 NP455009.RAGp0ULkWdc7KtMQvbde3UAdZMSN1oryMXt5_BcAcD_ew130_provenance.
- NP455009.RAGp0ULkWdc7KtMQvbde3UAdZMSN1oryMXt5_BcAcD_ew130_assertion wasGeneratedBy ECO_0000203 NP455009.RAGp0ULkWdc7KtMQvbde3UAdZMSN1oryMXt5_BcAcD_ew130_provenance.
- befree-20140225 importedOn "2014-02-25" NP455009.RAGp0ULkWdc7KtMQvbde3UAdZMSN1oryMXt5_BcAcD_ew130_provenance.