Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718361.RAVrwirjtglZ3bLWsoYXOL8cpLyEXwz4DcTyDxyFZmJLE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718361.RAVrwirjtglZ3bLWsoYXOL8cpLyEXwz4DcTyDxyFZmJLE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718361.RAVrwirjtglZ3bLWsoYXOL8cpLyEXwz4DcTyDxyFZmJLE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718361.RAVrwirjtglZ3bLWsoYXOL8cpLyEXwz4DcTyDxyFZmJLE130_provenance.
- NP718361.RAVrwirjtglZ3bLWsoYXOL8cpLyEXwz4DcTyDxyFZmJLE130_assertion description "[We developed amplification primers for most of the coding region and 3'-untranslated region of VLDLR and used sequencing of genomic DNA to examine these regions of VLDLR in subjects with familial combined hyperlipidemia and in normal controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718361.RAVrwirjtglZ3bLWsoYXOL8cpLyEXwz4DcTyDxyFZmJLE130_provenance.
- NP718361.RAVrwirjtglZ3bLWsoYXOL8cpLyEXwz4DcTyDxyFZmJLE130_assertion evidence source_evidence_literature NP718361.RAVrwirjtglZ3bLWsoYXOL8cpLyEXwz4DcTyDxyFZmJLE130_provenance.
- NP718361.RAVrwirjtglZ3bLWsoYXOL8cpLyEXwz4DcTyDxyFZmJLE130_assertion SIO_000772 11501949 NP718361.RAVrwirjtglZ3bLWsoYXOL8cpLyEXwz4DcTyDxyFZmJLE130_provenance.
- NP718361.RAVrwirjtglZ3bLWsoYXOL8cpLyEXwz4DcTyDxyFZmJLE130_assertion wasDerivedFrom befree-20140225 NP718361.RAVrwirjtglZ3bLWsoYXOL8cpLyEXwz4DcTyDxyFZmJLE130_provenance.
- NP718361.RAVrwirjtglZ3bLWsoYXOL8cpLyEXwz4DcTyDxyFZmJLE130_assertion wasGeneratedBy ECO_0000203 NP718361.RAVrwirjtglZ3bLWsoYXOL8cpLyEXwz4DcTyDxyFZmJLE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718361.RAVrwirjtglZ3bLWsoYXOL8cpLyEXwz4DcTyDxyFZmJLE130_provenance.