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- NP631416.RAGfERsR_l6fQSkUmVEGV-Md73jwW4r3l633SsC4u6uWo130_assertion type Assertion NP631416.RAGfERsR_l6fQSkUmVEGV-Md73jwW4r3l633SsC4u6uWo130_head.
- NP631416.RAGfERsR_l6fQSkUmVEGV-Md73jwW4r3l633SsC4u6uWo130_assertion description "[Mutations of the transforming growth factor beta (TGFbeta) receptor components ENDOGLIN and ALK-1 cause the autosomal dominant vascular disorder hereditary haemorrhagic telangiectasia (HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631416.RAGfERsR_l6fQSkUmVEGV-Md73jwW4r3l633SsC4u6uWo130_provenance.
- NP631416.RAGfERsR_l6fQSkUmVEGV-Md73jwW4r3l633SsC4u6uWo130_assertion evidence source_evidence_literature NP631416.RAGfERsR_l6fQSkUmVEGV-Md73jwW4r3l633SsC4u6uWo130_provenance.
- NP631416.RAGfERsR_l6fQSkUmVEGV-Md73jwW4r3l633SsC4u6uWo130_assertion SIO_000772 14684682 NP631416.RAGfERsR_l6fQSkUmVEGV-Md73jwW4r3l633SsC4u6uWo130_provenance.
- NP631416.RAGfERsR_l6fQSkUmVEGV-Md73jwW4r3l633SsC4u6uWo130_assertion wasDerivedFrom befree-20140225 NP631416.RAGfERsR_l6fQSkUmVEGV-Md73jwW4r3l633SsC4u6uWo130_provenance.
- NP631416.RAGfERsR_l6fQSkUmVEGV-Md73jwW4r3l633SsC4u6uWo130_assertion wasGeneratedBy ECO_0000203 NP631416.RAGfERsR_l6fQSkUmVEGV-Md73jwW4r3l633SsC4u6uWo130_provenance.