Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP584741.RA_htZ_yFycfPjMh3Gk2Sh-J8gg5Ak0OxGwjFm53LWXi4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584741.RA_htZ_yFycfPjMh3Gk2Sh-J8gg5Ak0OxGwjFm53LWXi4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584741.RA_htZ_yFycfPjMh3Gk2Sh-J8gg5Ak0OxGwjFm53LWXi4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584741.RA_htZ_yFycfPjMh3Gk2Sh-J8gg5Ak0OxGwjFm53LWXi4130_provenance.
- NP584741.RA_htZ_yFycfPjMh3Gk2Sh-J8gg5Ak0OxGwjFm53LWXi4130_assertion description "[The data are consistent with robust transcription of FTL in the lens, and suggest that whereas variations clustered in the IRE of the FTL gene are directly associated with hereditary hyperferritinemia-cataract syndrome, such IRE variations are unlikely to play a significant role in the genetic etiology of age-related cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584741.RA_htZ_yFycfPjMh3Gk2Sh-J8gg5Ak0OxGwjFm53LWXi4130_provenance.
- NP584741.RA_htZ_yFycfPjMh3Gk2Sh-J8gg5Ak0OxGwjFm53LWXi4130_assertion evidence source_evidence_literature NP584741.RA_htZ_yFycfPjMh3Gk2Sh-J8gg5Ak0OxGwjFm53LWXi4130_provenance.
- NP584741.RA_htZ_yFycfPjMh3Gk2Sh-J8gg5Ak0OxGwjFm53LWXi4130_assertion SIO_000772 23592921 NP584741.RA_htZ_yFycfPjMh3Gk2Sh-J8gg5Ak0OxGwjFm53LWXi4130_provenance.
- NP584741.RA_htZ_yFycfPjMh3Gk2Sh-J8gg5Ak0OxGwjFm53LWXi4130_assertion wasDerivedFrom befree-20140225 NP584741.RA_htZ_yFycfPjMh3Gk2Sh-J8gg5Ak0OxGwjFm53LWXi4130_provenance.
- NP584741.RA_htZ_yFycfPjMh3Gk2Sh-J8gg5Ak0OxGwjFm53LWXi4130_assertion wasGeneratedBy ECO_0000203 NP584741.RA_htZ_yFycfPjMh3Gk2Sh-J8gg5Ak0OxGwjFm53LWXi4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP584741.RA_htZ_yFycfPjMh3Gk2Sh-J8gg5Ak0OxGwjFm53LWXi4130_provenance.