Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP238906.RAJHHtuQNspMzmVKjEcP25z0fTimFeCwuo5fYLlp9OJSA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP238906.RAJHHtuQNspMzmVKjEcP25z0fTimFeCwuo5fYLlp9OJSA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP238906.RAJHHtuQNspMzmVKjEcP25z0fTimFeCwuo5fYLlp9OJSA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP238906.RAJHHtuQNspMzmVKjEcP25z0fTimFeCwuo5fYLlp9OJSA130_provenance.
- NP238906.RAJHHtuQNspMzmVKjEcP25z0fTimFeCwuo5fYLlp9OJSA130_assertion description "[These data provide the first direct evidence that MCKD2 and FJHN arise from mutation of the UMOD gene and are allelic disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP238906.RAJHHtuQNspMzmVKjEcP25z0fTimFeCwuo5fYLlp9OJSA130_provenance.
- NP238906.RAJHHtuQNspMzmVKjEcP25z0fTimFeCwuo5fYLlp9OJSA130_assertion evidence source_evidence_literature NP238906.RAJHHtuQNspMzmVKjEcP25z0fTimFeCwuo5fYLlp9OJSA130_provenance.
- NP238906.RAJHHtuQNspMzmVKjEcP25z0fTimFeCwuo5fYLlp9OJSA130_assertion SIO_000772 12471200 NP238906.RAJHHtuQNspMzmVKjEcP25z0fTimFeCwuo5fYLlp9OJSA130_provenance.
- NP238906.RAJHHtuQNspMzmVKjEcP25z0fTimFeCwuo5fYLlp9OJSA130_assertion wasDerivedFrom befree-20140225 NP238906.RAJHHtuQNspMzmVKjEcP25z0fTimFeCwuo5fYLlp9OJSA130_provenance.
- NP238906.RAJHHtuQNspMzmVKjEcP25z0fTimFeCwuo5fYLlp9OJSA130_assertion wasGeneratedBy ECO_0000203 NP238906.RAJHHtuQNspMzmVKjEcP25z0fTimFeCwuo5fYLlp9OJSA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP238906.RAJHHtuQNspMzmVKjEcP25z0fTimFeCwuo5fYLlp9OJSA130_provenance.