Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_assertion> ?p ?o ?g. }
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- NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_assertion type Assertion NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_head.
- NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_assertion wasGeneratedBy ECO_0000203 NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_provenance.
- NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_assertion wasDerivedFrom befree-20150227 NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_provenance.
- NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_assertion SIO_000772 12734540 NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_provenance.
- NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_assertion evidence source_evidence_literature NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_provenance.
- NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_assertion description "[Germline mutations in the RET proto-oncogene are responsible for the development of human hereditary diseases, including multiple endocrine neoplasia (MEN) type 2A and 2B, familial medullary thyroid carcinoma (FMTC), and Hirschsprung's disease (HSCR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_provenance.