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- NP676671.RAIWci9jT-CE-BRGbCc8C4UoGygWn1gk49fSR5BZZiF2s130_assertion type Assertion NP676671.RAIWci9jT-CE-BRGbCc8C4UoGygWn1gk49fSR5BZZiF2s130_head.
- NP676671.RAIWci9jT-CE-BRGbCc8C4UoGygWn1gk49fSR5BZZiF2s130_assertion wasGeneratedBy ECO_0000203 NP676671.RAIWci9jT-CE-BRGbCc8C4UoGygWn1gk49fSR5BZZiF2s130_provenance.
- NP676671.RAIWci9jT-CE-BRGbCc8C4UoGygWn1gk49fSR5BZZiF2s130_assertion wasDerivedFrom befree-2016 NP676671.RAIWci9jT-CE-BRGbCc8C4UoGygWn1gk49fSR5BZZiF2s130_provenance.
- NP676671.RAIWci9jT-CE-BRGbCc8C4UoGygWn1gk49fSR5BZZiF2s130_assertion SIO_000772 18554279 NP676671.RAIWci9jT-CE-BRGbCc8C4UoGygWn1gk49fSR5BZZiF2s130_provenance.
- NP676671.RAIWci9jT-CE-BRGbCc8C4UoGygWn1gk49fSR5BZZiF2s130_assertion evidence source_evidence_literature NP676671.RAIWci9jT-CE-BRGbCc8C4UoGygWn1gk49fSR5BZZiF2s130_provenance.
- NP676671.RAIWci9jT-CE-BRGbCc8C4UoGygWn1gk49fSR5BZZiF2s130_assertion description "[A heterozygous single base mutation in the human growth hormone (GH) gene (GH-1) was identified in a family presenting with isolated GH deficiency type II (IGHD II).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676671.RAIWci9jT-CE-BRGbCc8C4UoGygWn1gk49fSR5BZZiF2s130_provenance.