Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP734401.RAe5QNgjjQrPx8wLwcdBWrb_cwBHJmt0Vy9P0K9JoXtgI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP734401.RAe5QNgjjQrPx8wLwcdBWrb_cwBHJmt0Vy9P0K9JoXtgI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734401.RAe5QNgjjQrPx8wLwcdBWrb_cwBHJmt0Vy9P0K9JoXtgI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734401.RAe5QNgjjQrPx8wLwcdBWrb_cwBHJmt0Vy9P0K9JoXtgI130_provenance.
- NP734401.RAe5QNgjjQrPx8wLwcdBWrb_cwBHJmt0Vy9P0K9JoXtgI130_assertion description "[Mutations in the genes encoding transforming growth factor-beta receptor types I and II (TGFBR1 and TGFBR2, respectively) are commonly identified in patients with Loeys-Dietz syndrome, as well as some patients with Marfan's syndrome or familial thoracic aortic aneurysms and dissections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734401.RAe5QNgjjQrPx8wLwcdBWrb_cwBHJmt0Vy9P0K9JoXtgI130_provenance.
- NP734401.RAe5QNgjjQrPx8wLwcdBWrb_cwBHJmt0Vy9P0K9JoXtgI130_assertion evidence source_evidence_literature NP734401.RAe5QNgjjQrPx8wLwcdBWrb_cwBHJmt0Vy9P0K9JoXtgI130_provenance.
- NP734401.RAe5QNgjjQrPx8wLwcdBWrb_cwBHJmt0Vy9P0K9JoXtgI130_assertion SIO_000772 18721526 NP734401.RAe5QNgjjQrPx8wLwcdBWrb_cwBHJmt0Vy9P0K9JoXtgI130_provenance.
- NP734401.RAe5QNgjjQrPx8wLwcdBWrb_cwBHJmt0Vy9P0K9JoXtgI130_assertion wasDerivedFrom befree-20150227 NP734401.RAe5QNgjjQrPx8wLwcdBWrb_cwBHJmt0Vy9P0K9JoXtgI130_provenance.
- NP734401.RAe5QNgjjQrPx8wLwcdBWrb_cwBHJmt0Vy9P0K9JoXtgI130_assertion wasGeneratedBy ECO_0000203 NP734401.RAe5QNgjjQrPx8wLwcdBWrb_cwBHJmt0Vy9P0K9JoXtgI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP734401.RAe5QNgjjQrPx8wLwcdBWrb_cwBHJmt0Vy9P0K9JoXtgI130_provenance.