Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_assertion> ?p ?o ?g. }
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- NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_assertion type Assertion NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_head.
- NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_assertion description "[A questionnaire based study provides evidence that the hereditary hemorrhagic telangiectasia (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." NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_provenance.
- NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_assertion evidence source_evidence_literature NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_provenance.
- NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_assertion SIO_000772 12920067 NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_provenance.
- NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_assertion wasDerivedFrom lhgdn-20090331 NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_provenance.
- NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_assertion wasGeneratedBy ECO_0000203 NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_provenance.