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- NP100931.RAwXpnbOn8fkHzRDr6_JpEo2ggfVApUhptgj3goqe8RJ4130_assertion type Assertion NP100931.RAwXpnbOn8fkHzRDr6_JpEo2ggfVApUhptgj3goqe8RJ4130_head.
- NP100931.RAwXpnbOn8fkHzRDr6_JpEo2ggfVApUhptgj3goqe8RJ4130_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." NP100931.RAwXpnbOn8fkHzRDr6_JpEo2ggfVApUhptgj3goqe8RJ4130_provenance.
- NP100931.RAwXpnbOn8fkHzRDr6_JpEo2ggfVApUhptgj3goqe8RJ4130_assertion evidence source_evidence_literature NP100931.RAwXpnbOn8fkHzRDr6_JpEo2ggfVApUhptgj3goqe8RJ4130_provenance.
- NP100931.RAwXpnbOn8fkHzRDr6_JpEo2ggfVApUhptgj3goqe8RJ4130_assertion SIO_000772 16752392 NP100931.RAwXpnbOn8fkHzRDr6_JpEo2ggfVApUhptgj3goqe8RJ4130_provenance.
- NP100931.RAwXpnbOn8fkHzRDr6_JpEo2ggfVApUhptgj3goqe8RJ4130_assertion wasDerivedFrom gad-20150221 NP100931.RAwXpnbOn8fkHzRDr6_JpEo2ggfVApUhptgj3goqe8RJ4130_provenance.
- NP100931.RAwXpnbOn8fkHzRDr6_JpEo2ggfVApUhptgj3goqe8RJ4130_assertion wasGeneratedBy ECO_0000203 NP100931.RAwXpnbOn8fkHzRDr6_JpEo2ggfVApUhptgj3goqe8RJ4130_provenance.