Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP239723.RAQ3vBMIKZ-91cdnwRb7vdbXOq5jrzJZg3WNtNexl5HG0130_assertion> ?p ?o ?g. }
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- NP239723.RAQ3vBMIKZ-91cdnwRb7vdbXOq5jrzJZg3WNtNexl5HG0130_assertion type Assertion NP239723.RAQ3vBMIKZ-91cdnwRb7vdbXOq5jrzJZg3WNtNexl5HG0130_head.
- NP239723.RAQ3vBMIKZ-91cdnwRb7vdbXOq5jrzJZg3WNtNexl5HG0130_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." NP239723.RAQ3vBMIKZ-91cdnwRb7vdbXOq5jrzJZg3WNtNexl5HG0130_provenance.
- NP239723.RAQ3vBMIKZ-91cdnwRb7vdbXOq5jrzJZg3WNtNexl5HG0130_assertion evidence source_evidence_literature NP239723.RAQ3vBMIKZ-91cdnwRb7vdbXOq5jrzJZg3WNtNexl5HG0130_provenance.
- NP239723.RAQ3vBMIKZ-91cdnwRb7vdbXOq5jrzJZg3WNtNexl5HG0130_assertion SIO_000772 18607909 NP239723.RAQ3vBMIKZ-91cdnwRb7vdbXOq5jrzJZg3WNtNexl5HG0130_provenance.
- NP239723.RAQ3vBMIKZ-91cdnwRb7vdbXOq5jrzJZg3WNtNexl5HG0130_assertion wasDerivedFrom lhgdn-20090331 NP239723.RAQ3vBMIKZ-91cdnwRb7vdbXOq5jrzJZg3WNtNexl5HG0130_provenance.
- NP239723.RAQ3vBMIKZ-91cdnwRb7vdbXOq5jrzJZg3WNtNexl5HG0130_assertion wasGeneratedBy ECO_0000203 NP239723.RAQ3vBMIKZ-91cdnwRb7vdbXOq5jrzJZg3WNtNexl5HG0130_provenance.