Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP801355.RArZ_-tdhMtNvDjKwuXea7mspiIdWSbVG2GwNG-ai6Ne4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP801355.RArZ_-tdhMtNvDjKwuXea7mspiIdWSbVG2GwNG-ai6Ne4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP801355.RArZ_-tdhMtNvDjKwuXea7mspiIdWSbVG2GwNG-ai6Ne4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP801355.RArZ_-tdhMtNvDjKwuXea7mspiIdWSbVG2GwNG-ai6Ne4130_provenance.
- NP801355.RArZ_-tdhMtNvDjKwuXea7mspiIdWSbVG2GwNG-ai6Ne4130_assertion description "[The authors' objective is to report two heterozygous missense mutations in the NDUFAF1 gene as a cause of fatal infantile HCM in a patient with isolated complex I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801355.RArZ_-tdhMtNvDjKwuXea7mspiIdWSbVG2GwNG-ai6Ne4130_provenance.
- NP801355.RArZ_-tdhMtNvDjKwuXea7mspiIdWSbVG2GwNG-ai6Ne4130_assertion evidence source_evidence_literature NP801355.RArZ_-tdhMtNvDjKwuXea7mspiIdWSbVG2GwNG-ai6Ne4130_provenance.
- NP801355.RArZ_-tdhMtNvDjKwuXea7mspiIdWSbVG2GwNG-ai6Ne4130_assertion SIO_000772 21931170 NP801355.RArZ_-tdhMtNvDjKwuXea7mspiIdWSbVG2GwNG-ai6Ne4130_provenance.
- NP801355.RArZ_-tdhMtNvDjKwuXea7mspiIdWSbVG2GwNG-ai6Ne4130_assertion wasDerivedFrom befree-20140225 NP801355.RArZ_-tdhMtNvDjKwuXea7mspiIdWSbVG2GwNG-ai6Ne4130_provenance.
- NP801355.RArZ_-tdhMtNvDjKwuXea7mspiIdWSbVG2GwNG-ai6Ne4130_assertion wasGeneratedBy ECO_0000203 NP801355.RArZ_-tdhMtNvDjKwuXea7mspiIdWSbVG2GwNG-ai6Ne4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP801355.RArZ_-tdhMtNvDjKwuXea7mspiIdWSbVG2GwNG-ai6Ne4130_provenance.