Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP152705.RAKlboFsD-GFvwsm8GZ5fzQa0OyfE74f1nnW9DDp4asqU130_assertion> ?p ?o ?g. }
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- NP152705.RAKlboFsD-GFvwsm8GZ5fzQa0OyfE74f1nnW9DDp4asqU130_assertion type Assertion NP152705.RAKlboFsD-GFvwsm8GZ5fzQa0OyfE74f1nnW9DDp4asqU130_head.
- NP152705.RAKlboFsD-GFvwsm8GZ5fzQa0OyfE74f1nnW9DDp4asqU130_assertion description "[identified ACVRL1 mutations in hereditary hemorrhagic telangiectasia, including 4 unknown, and found that ACVRL1, and not ENG, mutations are predictive for liver disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152705.RAKlboFsD-GFvwsm8GZ5fzQa0OyfE74f1nnW9DDp4asqU130_provenance.
- NP152705.RAKlboFsD-GFvwsm8GZ5fzQa0OyfE74f1nnW9DDp4asqU130_assertion evidence source_evidence_literature NP152705.RAKlboFsD-GFvwsm8GZ5fzQa0OyfE74f1nnW9DDp4asqU130_provenance.
- NP152705.RAKlboFsD-GFvwsm8GZ5fzQa0OyfE74f1nnW9DDp4asqU130_assertion SIO_000772 18498373 NP152705.RAKlboFsD-GFvwsm8GZ5fzQa0OyfE74f1nnW9DDp4asqU130_provenance.
- NP152705.RAKlboFsD-GFvwsm8GZ5fzQa0OyfE74f1nnW9DDp4asqU130_assertion wasDerivedFrom lhgdn-20090331 NP152705.RAKlboFsD-GFvwsm8GZ5fzQa0OyfE74f1nnW9DDp4asqU130_provenance.
- NP152705.RAKlboFsD-GFvwsm8GZ5fzQa0OyfE74f1nnW9DDp4asqU130_assertion wasGeneratedBy ECO_0000203 NP152705.RAKlboFsD-GFvwsm8GZ5fzQa0OyfE74f1nnW9DDp4asqU130_provenance.