Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP554007.RA-4FMl6_EBXsCccEuR2vMW3eJGsmsL4UUYj6vCn3UQlo130_assertion> ?p ?o ?g. }
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- NP554007.RA-4FMl6_EBXsCccEuR2vMW3eJGsmsL4UUYj6vCn3UQlo130_assertion type Assertion NP554007.RA-4FMl6_EBXsCccEuR2vMW3eJGsmsL4UUYj6vCn3UQlo130_head.
- NP554007.RA-4FMl6_EBXsCccEuR2vMW3eJGsmsL4UUYj6vCn3UQlo130_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." NP554007.RA-4FMl6_EBXsCccEuR2vMW3eJGsmsL4UUYj6vCn3UQlo130_provenance.
- NP554007.RA-4FMl6_EBXsCccEuR2vMW3eJGsmsL4UUYj6vCn3UQlo130_assertion evidence source_evidence_literature NP554007.RA-4FMl6_EBXsCccEuR2vMW3eJGsmsL4UUYj6vCn3UQlo130_provenance.
- NP554007.RA-4FMl6_EBXsCccEuR2vMW3eJGsmsL4UUYj6vCn3UQlo130_assertion SIO_000772 17527005 NP554007.RA-4FMl6_EBXsCccEuR2vMW3eJGsmsL4UUYj6vCn3UQlo130_provenance.
- NP554007.RA-4FMl6_EBXsCccEuR2vMW3eJGsmsL4UUYj6vCn3UQlo130_assertion wasDerivedFrom befree-20140225 NP554007.RA-4FMl6_EBXsCccEuR2vMW3eJGsmsL4UUYj6vCn3UQlo130_provenance.
- NP554007.RA-4FMl6_EBXsCccEuR2vMW3eJGsmsL4UUYj6vCn3UQlo130_assertion wasGeneratedBy ECO_0000203 NP554007.RA-4FMl6_EBXsCccEuR2vMW3eJGsmsL4UUYj6vCn3UQlo130_provenance.