Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_assertion type Assertion NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_head.
- NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_assertion description "[Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_provenance.
- NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_assertion evidence source_evidence_literature NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_provenance.
- NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_assertion SIO_000772 19085907 NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_provenance.
- NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_assertion wasDerivedFrom befree-2016 NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_provenance.
- NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_assertion wasGeneratedBy ECO_0000203 NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_provenance.