Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP2457.RAAovslGwUwt1SG2nYdZgdZvvw_4fl6HRoraSM4F6v2bg130_assertion> ?p ?o ?g. }
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- NP2457.RAAovslGwUwt1SG2nYdZgdZvvw_4fl6HRoraSM4F6v2bg130_assertion type Assertion NP2457.RAAovslGwUwt1SG2nYdZgdZvvw_4fl6HRoraSM4F6v2bg130_head.
- NP2457.RAAovslGwUwt1SG2nYdZgdZvvw_4fl6HRoraSM4F6v2bg130_assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2457.RAAovslGwUwt1SG2nYdZgdZvvw_4fl6HRoraSM4F6v2bg130_provenance.
- NP2457.RAAovslGwUwt1SG2nYdZgdZvvw_4fl6HRoraSM4F6v2bg130_assertion evidence source_evidence_curated NP2457.RAAovslGwUwt1SG2nYdZgdZvvw_4fl6HRoraSM4F6v2bg130_provenance.
- NP2457.RAAovslGwUwt1SG2nYdZgdZvvw_4fl6HRoraSM4F6v2bg130_assertion SIO_000772 16752392 NP2457.RAAovslGwUwt1SG2nYdZgdZvvw_4fl6HRoraSM4F6v2bg130_provenance.
- NP2457.RAAovslGwUwt1SG2nYdZgdZvvw_4fl6HRoraSM4F6v2bg130_assertion wasDerivedFrom uniprot-20150221 NP2457.RAAovslGwUwt1SG2nYdZgdZvvw_4fl6HRoraSM4F6v2bg130_provenance.
- NP2457.RAAovslGwUwt1SG2nYdZgdZvvw_4fl6HRoraSM4F6v2bg130_assertion wasGeneratedBy ECO_0000218 NP2457.RAAovslGwUwt1SG2nYdZgdZvvw_4fl6HRoraSM4F6v2bg130_provenance.