Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP661347.RAV9flvq7hf_Lss5ug4FMaYsIYn21kv0mz_MuH1_yd69w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP661347.RAV9flvq7hf_Lss5ug4FMaYsIYn21kv0mz_MuH1_yd69w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP661347.RAV9flvq7hf_Lss5ug4FMaYsIYn21kv0mz_MuH1_yd69w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP661347.RAV9flvq7hf_Lss5ug4FMaYsIYn21kv0mz_MuH1_yd69w130_provenance.
- NP661347.RAV9flvq7hf_Lss5ug4FMaYsIYn21kv0mz_MuH1_yd69w130_assertion description "[This study was conducted to report a family affected by benign hereditary chorea in which a large deletion including TTF1, PAX9, and other genes was identified and results in oligodontia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661347.RAV9flvq7hf_Lss5ug4FMaYsIYn21kv0mz_MuH1_yd69w130_provenance.
- NP661347.RAV9flvq7hf_Lss5ug4FMaYsIYn21kv0mz_MuH1_yd69w130_assertion evidence source_evidence_literature NP661347.RAV9flvq7hf_Lss5ug4FMaYsIYn21kv0mz_MuH1_yd69w130_provenance.
- NP661347.RAV9flvq7hf_Lss5ug4FMaYsIYn21kv0mz_MuH1_yd69w130_assertion SIO_000772 18445003 NP661347.RAV9flvq7hf_Lss5ug4FMaYsIYn21kv0mz_MuH1_yd69w130_provenance.
- NP661347.RAV9flvq7hf_Lss5ug4FMaYsIYn21kv0mz_MuH1_yd69w130_assertion wasDerivedFrom befree-20140225 NP661347.RAV9flvq7hf_Lss5ug4FMaYsIYn21kv0mz_MuH1_yd69w130_provenance.
- NP661347.RAV9flvq7hf_Lss5ug4FMaYsIYn21kv0mz_MuH1_yd69w130_assertion wasGeneratedBy ECO_0000203 NP661347.RAV9flvq7hf_Lss5ug4FMaYsIYn21kv0mz_MuH1_yd69w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP661347.RAV9flvq7hf_Lss5ug4FMaYsIYn21kv0mz_MuH1_yd69w130_provenance.