Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP182635.RATGy6qHpceYzbCy16s1o6Srt6SlYP6IxcF9_IJsWpxFE130_assertion> ?p ?o ?g. }
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- NP182635.RATGy6qHpceYzbCy16s1o6Srt6SlYP6IxcF9_IJsWpxFE130_assertion type Assertion NP182635.RATGy6qHpceYzbCy16s1o6Srt6SlYP6IxcF9_IJsWpxFE130_head.
- NP182635.RATGy6qHpceYzbCy16s1o6Srt6SlYP6IxcF9_IJsWpxFE130_assertion description "[Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182635.RATGy6qHpceYzbCy16s1o6Srt6SlYP6IxcF9_IJsWpxFE130_provenance.
- NP182635.RATGy6qHpceYzbCy16s1o6Srt6SlYP6IxcF9_IJsWpxFE130_assertion evidence source_evidence_literature NP182635.RATGy6qHpceYzbCy16s1o6Srt6SlYP6IxcF9_IJsWpxFE130_provenance.
- NP182635.RATGy6qHpceYzbCy16s1o6Srt6SlYP6IxcF9_IJsWpxFE130_assertion SIO_000772 12920067 NP182635.RATGy6qHpceYzbCy16s1o6Srt6SlYP6IxcF9_IJsWpxFE130_provenance.
- NP182635.RATGy6qHpceYzbCy16s1o6Srt6SlYP6IxcF9_IJsWpxFE130_assertion wasDerivedFrom befree-20140225 NP182635.RATGy6qHpceYzbCy16s1o6Srt6SlYP6IxcF9_IJsWpxFE130_provenance.
- NP182635.RATGy6qHpceYzbCy16s1o6Srt6SlYP6IxcF9_IJsWpxFE130_assertion wasGeneratedBy ECO_0000203 NP182635.RATGy6qHpceYzbCy16s1o6Srt6SlYP6IxcF9_IJsWpxFE130_provenance.