Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP374820.RAo8uImuE-UwbZhXcfFzqFgGhfQRFE5tFgCesxkDuW7TY130_assertion> ?p ?o ?g. }
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- NP374820.RAo8uImuE-UwbZhXcfFzqFgGhfQRFE5tFgCesxkDuW7TY130_assertion type Assertion NP374820.RAo8uImuE-UwbZhXcfFzqFgGhfQRFE5tFgCesxkDuW7TY130_head.
- NP374820.RAo8uImuE-UwbZhXcfFzqFgGhfQRFE5tFgCesxkDuW7TY130_assertion wasGeneratedBy ECO_0000203 NP374820.RAo8uImuE-UwbZhXcfFzqFgGhfQRFE5tFgCesxkDuW7TY130_provenance.
- NP374820.RAo8uImuE-UwbZhXcfFzqFgGhfQRFE5tFgCesxkDuW7TY130_assertion wasDerivedFrom befree-20150227 NP374820.RAo8uImuE-UwbZhXcfFzqFgGhfQRFE5tFgCesxkDuW7TY130_provenance.
- NP374820.RAo8uImuE-UwbZhXcfFzqFgGhfQRFE5tFgCesxkDuW7TY130_assertion SIO_000772 16470787 NP374820.RAo8uImuE-UwbZhXcfFzqFgGhfQRFE5tFgCesxkDuW7TY130_provenance.
- NP374820.RAo8uImuE-UwbZhXcfFzqFgGhfQRFE5tFgCesxkDuW7TY130_assertion evidence source_evidence_literature NP374820.RAo8uImuE-UwbZhXcfFzqFgGhfQRFE5tFgCesxkDuW7TY130_provenance.
- NP374820.RAo8uImuE-UwbZhXcfFzqFgGhfQRFE5tFgCesxkDuW7TY130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is a genetically heterogeneous vascular dysplasia with multiple telangiectases and arteriovenous malformations and it is caused by mutations in endoglin gene (ENG) (HHT1) and activin A receptor type II-like 1 gene (ACVRL1) (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374820.RAo8uImuE-UwbZhXcfFzqFgGhfQRFE5tFgCesxkDuW7TY130_provenance.