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- NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_assertion type Assertion NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_head.
- NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT), the most common inherited vascular disorder, is caused by mutations in genes involved in�the transforming growth factor beta (TGF-?) signaling pathway (ENG, ACVRL1, and SMAD4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_provenance.
- NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_assertion evidence source_evidence_literature NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_provenance.
- NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_assertion SIO_000772 23972370 NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_provenance.
- NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_assertion wasDerivedFrom befree-20140225 NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_provenance.
- NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_assertion wasGeneratedBy ECO_0000203 NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_provenance.