Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_assertion> ?p ?o ?g. }
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- NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_assertion type Assertion NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_head.
- NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_assertion description "[Our questionnaire based study provides evidence that the HHT phenotype caused by mutations in endoglin (HHT1) is distinct from, and more severe than, HHT caused by mutations in ALK1 (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_provenance.
- NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_assertion evidence source_evidence_literature NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_provenance.
- NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_assertion SIO_000772 12920067 NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_provenance.
- NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_assertion wasDerivedFrom gad-20130706 NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_provenance.
- NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_assertion wasGeneratedBy ECO_0000203 NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_provenance.