Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP644530.RAGyzv9eTeL_mhUJrydXlfMmwuCEuwX0Xp7Y_9jfnRMx4130_assertion> ?p ?o ?g. }
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- NP644530.RAGyzv9eTeL_mhUJrydXlfMmwuCEuwX0Xp7Y_9jfnRMx4130_assertion type Assertion NP644530.RAGyzv9eTeL_mhUJrydXlfMmwuCEuwX0Xp7Y_9jfnRMx4130_head.
- NP644530.RAGyzv9eTeL_mhUJrydXlfMmwuCEuwX0Xp7Y_9jfnRMx4130_assertion wasGeneratedBy ECO_0000203 NP644530.RAGyzv9eTeL_mhUJrydXlfMmwuCEuwX0Xp7Y_9jfnRMx4130_provenance.
- NP644530.RAGyzv9eTeL_mhUJrydXlfMmwuCEuwX0Xp7Y_9jfnRMx4130_assertion wasDerivedFrom befree-20140225 NP644530.RAGyzv9eTeL_mhUJrydXlfMmwuCEuwX0Xp7Y_9jfnRMx4130_provenance.
- NP644530.RAGyzv9eTeL_mhUJrydXlfMmwuCEuwX0Xp7Y_9jfnRMx4130_assertion SIO_000772 10822217 NP644530.RAGyzv9eTeL_mhUJrydXlfMmwuCEuwX0Xp7Y_9jfnRMx4130_provenance.
- NP644530.RAGyzv9eTeL_mhUJrydXlfMmwuCEuwX0Xp7Y_9jfnRMx4130_assertion evidence source_evidence_literature NP644530.RAGyzv9eTeL_mhUJrydXlfMmwuCEuwX0Xp7Y_9jfnRMx4130_provenance.
- NP644530.RAGyzv9eTeL_mhUJrydXlfMmwuCEuwX0Xp7Y_9jfnRMx4130_assertion description "[FGHD due to an autosomal recessive GHRH-R gene mutation leads to marked dwarfism, phenotypically and hormonally indistinguishable from other forms of isolated GH deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP644530.RAGyzv9eTeL_mhUJrydXlfMmwuCEuwX0Xp7Y_9jfnRMx4130_provenance.