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- source_evidence_literature type ECO_0000212 NP611921.RAYyCEDGl1yxnn5heSztkggwlFTFELGXvppC8xEcRxs80130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP611921.RAYyCEDGl1yxnn5heSztkggwlFTFELGXvppC8xEcRxs80130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP611921.RAYyCEDGl1yxnn5heSztkggwlFTFELGXvppC8xEcRxs80130_provenance.
- NP611921.RAYyCEDGl1yxnn5heSztkggwlFTFELGXvppC8xEcRxs80130_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." NP611921.RAYyCEDGl1yxnn5heSztkggwlFTFELGXvppC8xEcRxs80130_provenance.
- NP611921.RAYyCEDGl1yxnn5heSztkggwlFTFELGXvppC8xEcRxs80130_assertion evidence source_evidence_literature NP611921.RAYyCEDGl1yxnn5heSztkggwlFTFELGXvppC8xEcRxs80130_provenance.
- NP611921.RAYyCEDGl1yxnn5heSztkggwlFTFELGXvppC8xEcRxs80130_assertion SIO_000772 17527005 NP611921.RAYyCEDGl1yxnn5heSztkggwlFTFELGXvppC8xEcRxs80130_provenance.
- NP611921.RAYyCEDGl1yxnn5heSztkggwlFTFELGXvppC8xEcRxs80130_assertion wasDerivedFrom befree-2016 NP611921.RAYyCEDGl1yxnn5heSztkggwlFTFELGXvppC8xEcRxs80130_provenance.
- NP611921.RAYyCEDGl1yxnn5heSztkggwlFTFELGXvppC8xEcRxs80130_assertion wasGeneratedBy ECO_0000203 NP611921.RAYyCEDGl1yxnn5heSztkggwlFTFELGXvppC8xEcRxs80130_provenance.
- befree-2016 importedOn "2016-02-19" NP611921.RAYyCEDGl1yxnn5heSztkggwlFTFELGXvppC8xEcRxs80130_provenance.