Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_provenance.