Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP401901.RASf8EBvtAaORZgxMG1jJEOI3fYOWiOSQoWMlMelpYoYE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401901.RASf8EBvtAaORZgxMG1jJEOI3fYOWiOSQoWMlMelpYoYE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401901.RASf8EBvtAaORZgxMG1jJEOI3fYOWiOSQoWMlMelpYoYE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401901.RASf8EBvtAaORZgxMG1jJEOI3fYOWiOSQoWMlMelpYoYE130_provenance.
- NP401901.RASf8EBvtAaORZgxMG1jJEOI3fYOWiOSQoWMlMelpYoYE130_assertion description "[Here we report a Japanese patient with CPHD (GH, PRL, TSH, LH, FSH, and ACTH deficiency) due to a novel missense mutation (P366T) of the LHX 4 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401901.RASf8EBvtAaORZgxMG1jJEOI3fYOWiOSQoWMlMelpYoYE130_provenance.
- NP401901.RASf8EBvtAaORZgxMG1jJEOI3fYOWiOSQoWMlMelpYoYE130_assertion evidence source_evidence_literature NP401901.RASf8EBvtAaORZgxMG1jJEOI3fYOWiOSQoWMlMelpYoYE130_provenance.
- NP401901.RASf8EBvtAaORZgxMG1jJEOI3fYOWiOSQoWMlMelpYoYE130_assertion SIO_000772 17527005 NP401901.RASf8EBvtAaORZgxMG1jJEOI3fYOWiOSQoWMlMelpYoYE130_provenance.
- NP401901.RASf8EBvtAaORZgxMG1jJEOI3fYOWiOSQoWMlMelpYoYE130_assertion wasDerivedFrom befree-20140225 NP401901.RASf8EBvtAaORZgxMG1jJEOI3fYOWiOSQoWMlMelpYoYE130_provenance.
- NP401901.RASf8EBvtAaORZgxMG1jJEOI3fYOWiOSQoWMlMelpYoYE130_assertion wasGeneratedBy ECO_0000203 NP401901.RASf8EBvtAaORZgxMG1jJEOI3fYOWiOSQoWMlMelpYoYE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP401901.RASf8EBvtAaORZgxMG1jJEOI3fYOWiOSQoWMlMelpYoYE130_provenance.