Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP491883.RAEp36VJkQLx1XX4SeJyEvbt0iMwwUQFj_yWttGH__vwc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP491883.RAEp36VJkQLx1XX4SeJyEvbt0iMwwUQFj_yWttGH__vwc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP491883.RAEp36VJkQLx1XX4SeJyEvbt0iMwwUQFj_yWttGH__vwc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP491883.RAEp36VJkQLx1XX4SeJyEvbt0iMwwUQFj_yWttGH__vwc130_provenance.
- NP491883.RAEp36VJkQLx1XX4SeJyEvbt0iMwwUQFj_yWttGH__vwc130_assertion description "[EKV3 is also characterized by ichthyosis, sensorineural hearing loss, peripheral neuropathy, psychomotor retardation, congenital chronic diarrhea, and an elevation of very long chain fatty acids (VLCFAs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491883.RAEp36VJkQLx1XX4SeJyEvbt0iMwwUQFj_yWttGH__vwc130_provenance.
- NP491883.RAEp36VJkQLx1XX4SeJyEvbt0iMwwUQFj_yWttGH__vwc130_assertion evidence source_evidence_literature NP491883.RAEp36VJkQLx1XX4SeJyEvbt0iMwwUQFj_yWttGH__vwc130_provenance.
- NP491883.RAEp36VJkQLx1XX4SeJyEvbt0iMwwUQFj_yWttGH__vwc130_assertion SIO_000772 15668823 NP491883.RAEp36VJkQLx1XX4SeJyEvbt0iMwwUQFj_yWttGH__vwc130_provenance.
- NP491883.RAEp36VJkQLx1XX4SeJyEvbt0iMwwUQFj_yWttGH__vwc130_assertion wasDerivedFrom befree-20140225 NP491883.RAEp36VJkQLx1XX4SeJyEvbt0iMwwUQFj_yWttGH__vwc130_provenance.
- NP491883.RAEp36VJkQLx1XX4SeJyEvbt0iMwwUQFj_yWttGH__vwc130_assertion wasGeneratedBy ECO_0000203 NP491883.RAEp36VJkQLx1XX4SeJyEvbt0iMwwUQFj_yWttGH__vwc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP491883.RAEp36VJkQLx1XX4SeJyEvbt0iMwwUQFj_yWttGH__vwc130_provenance.