Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP60602.RAGG902l1OQtW_-6i5uEv9OCvKzuTEctxGHgW-g5Ue9u4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP60602.RAGG902l1OQtW_-6i5uEv9OCvKzuTEctxGHgW-g5Ue9u4130_assertion type Assertion NP60602.RAGG902l1OQtW_-6i5uEv9OCvKzuTEctxGHgW-g5Ue9u4130_head.
- NP60602.RAGG902l1OQtW_-6i5uEv9OCvKzuTEctxGHgW-g5Ue9u4130_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." NP60602.RAGG902l1OQtW_-6i5uEv9OCvKzuTEctxGHgW-g5Ue9u4130_provenance.
- NP60602.RAGG902l1OQtW_-6i5uEv9OCvKzuTEctxGHgW-g5Ue9u4130_assertion evidence source_evidence_literature NP60602.RAGG902l1OQtW_-6i5uEv9OCvKzuTEctxGHgW-g5Ue9u4130_provenance.
- NP60602.RAGG902l1OQtW_-6i5uEv9OCvKzuTEctxGHgW-g5Ue9u4130_assertion SIO_000772 16752392 NP60602.RAGG902l1OQtW_-6i5uEv9OCvKzuTEctxGHgW-g5Ue9u4130_provenance.
- NP60602.RAGG902l1OQtW_-6i5uEv9OCvKzuTEctxGHgW-g5Ue9u4130_assertion wasDerivedFrom gad-20150221 NP60602.RAGG902l1OQtW_-6i5uEv9OCvKzuTEctxGHgW-g5Ue9u4130_provenance.
- NP60602.RAGG902l1OQtW_-6i5uEv9OCvKzuTEctxGHgW-g5Ue9u4130_assertion wasGeneratedBy ECO_0000203 NP60602.RAGG902l1OQtW_-6i5uEv9OCvKzuTEctxGHgW-g5Ue9u4130_provenance.