Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_provenance.
- NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_assertion description "[Recessively inherited deficiency of TH was recently identified and incorporated into recent concepts of genetic dystonias as the cause of recessive Dopa-responsive dystonia or Segawa's syndrome in analogy to dominantly inherited GTP cyclohydrolase I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_provenance.
- NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_assertion evidence source_evidence_literature NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_provenance.
- NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_assertion SIO_000772 12891655 NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_provenance.
- NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_assertion wasDerivedFrom befree-20150227 NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_provenance.
- NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_assertion wasGeneratedBy ECO_0000203 NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_provenance.