Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP461555.RAXFxeOAmlJEfMlyJCIS6hpgvyv3Y0c9R8hNvA2wr9DG4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP461555.RAXFxeOAmlJEfMlyJCIS6hpgvyv3Y0c9R8hNvA2wr9DG4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP461555.RAXFxeOAmlJEfMlyJCIS6hpgvyv3Y0c9R8hNvA2wr9DG4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP461555.RAXFxeOAmlJEfMlyJCIS6hpgvyv3Y0c9R8hNvA2wr9DG4130_provenance.
- NP461555.RAXFxeOAmlJEfMlyJCIS6hpgvyv3Y0c9R8hNvA2wr9DG4130_assertion description "[Phenotypic variability in Hey2 -/- mice and absence of HEY2 mutations in patients with congenital heart defects or Alagille syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461555.RAXFxeOAmlJEfMlyJCIS6hpgvyv3Y0c9R8hNvA2wr9DG4130_provenance.
- NP461555.RAXFxeOAmlJEfMlyJCIS6hpgvyv3Y0c9R8hNvA2wr9DG4130_assertion evidence source_evidence_literature NP461555.RAXFxeOAmlJEfMlyJCIS6hpgvyv3Y0c9R8hNvA2wr9DG4130_provenance.
- NP461555.RAXFxeOAmlJEfMlyJCIS6hpgvyv3Y0c9R8hNvA2wr9DG4130_assertion SIO_000772 15389319 NP461555.RAXFxeOAmlJEfMlyJCIS6hpgvyv3Y0c9R8hNvA2wr9DG4130_provenance.
- NP461555.RAXFxeOAmlJEfMlyJCIS6hpgvyv3Y0c9R8hNvA2wr9DG4130_assertion wasDerivedFrom befree-2016 NP461555.RAXFxeOAmlJEfMlyJCIS6hpgvyv3Y0c9R8hNvA2wr9DG4130_provenance.
- NP461555.RAXFxeOAmlJEfMlyJCIS6hpgvyv3Y0c9R8hNvA2wr9DG4130_assertion wasGeneratedBy ECO_0000203 NP461555.RAXFxeOAmlJEfMlyJCIS6hpgvyv3Y0c9R8hNvA2wr9DG4130_provenance.
- befree-2016 importedOn "2016-02-19" NP461555.RAXFxeOAmlJEfMlyJCIS6hpgvyv3Y0c9R8hNvA2wr9DG4130_provenance.