Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_provenance.
- NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_assertion description "[Hutchinson-Gilford Progeria Syndrome (HGPS) is a premature-aging syndrome caused by a dominant mutation in the gene encoding lamin A, which leads to an aberrantly spliced and processed protein termed progerin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_provenance.
- NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_assertion evidence source_evidence_literature NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_provenance.
- NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_assertion SIO_000772 20605919 NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_provenance.
- NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_assertion wasDerivedFrom befree-20140225 NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_provenance.
- NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_assertion wasGeneratedBy ECO_0000203 NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_provenance.