Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP215815.RAcoVyMO-djns7aIOegNWoX5EIrAPcRUpYbsDQou7B2nI130_assertion> ?p ?o ?g. }
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- NP215815.RAcoVyMO-djns7aIOegNWoX5EIrAPcRUpYbsDQou7B2nI130_assertion type Assertion NP215815.RAcoVyMO-djns7aIOegNWoX5EIrAPcRUpYbsDQou7B2nI130_head.
- NP215815.RAcoVyMO-djns7aIOegNWoX5EIrAPcRUpYbsDQou7B2nI130_assertion description "[in hereditary hemorrhagic telangiectasia all 4 ENG mutations and one of the ACVRL1 mutations were new and had not been described previously in other populations]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215815.RAcoVyMO-djns7aIOegNWoX5EIrAPcRUpYbsDQou7B2nI130_provenance.
- NP215815.RAcoVyMO-djns7aIOegNWoX5EIrAPcRUpYbsDQou7B2nI130_assertion evidence source_evidence_literature NP215815.RAcoVyMO-djns7aIOegNWoX5EIrAPcRUpYbsDQou7B2nI130_provenance.
- NP215815.RAcoVyMO-djns7aIOegNWoX5EIrAPcRUpYbsDQou7B2nI130_assertion SIO_000772 18607909 NP215815.RAcoVyMO-djns7aIOegNWoX5EIrAPcRUpYbsDQou7B2nI130_provenance.
- NP215815.RAcoVyMO-djns7aIOegNWoX5EIrAPcRUpYbsDQou7B2nI130_assertion wasDerivedFrom lhgdn-20090331 NP215815.RAcoVyMO-djns7aIOegNWoX5EIrAPcRUpYbsDQou7B2nI130_provenance.
- NP215815.RAcoVyMO-djns7aIOegNWoX5EIrAPcRUpYbsDQou7B2nI130_assertion wasGeneratedBy ECO_0000203 NP215815.RAcoVyMO-djns7aIOegNWoX5EIrAPcRUpYbsDQou7B2nI130_provenance.