Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3287.RAtBT-nKTHLHM4x8ieWLViB4XgXRJcJ7fZNwQwcz4H-1A130_assertion> ?p ?o ?g. }
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- NP3287.RAtBT-nKTHLHM4x8ieWLViB4XgXRJcJ7fZNwQwcz4H-1A130_assertion type Assertion NP3287.RAtBT-nKTHLHM4x8ieWLViB4XgXRJcJ7fZNwQwcz4H-1A130_head.
- NP3287.RAtBT-nKTHLHM4x8ieWLViB4XgXRJcJ7fZNwQwcz4H-1A130_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." NP3287.RAtBT-nKTHLHM4x8ieWLViB4XgXRJcJ7fZNwQwcz4H-1A130_provenance.
- NP3287.RAtBT-nKTHLHM4x8ieWLViB4XgXRJcJ7fZNwQwcz4H-1A130_assertion evidence source_evidence_curated NP3287.RAtBT-nKTHLHM4x8ieWLViB4XgXRJcJ7fZNwQwcz4H-1A130_provenance.
- NP3287.RAtBT-nKTHLHM4x8ieWLViB4XgXRJcJ7fZNwQwcz4H-1A130_assertion SIO_000772 19085907 NP3287.RAtBT-nKTHLHM4x8ieWLViB4XgXRJcJ7fZNwQwcz4H-1A130_provenance.
- NP3287.RAtBT-nKTHLHM4x8ieWLViB4XgXRJcJ7fZNwQwcz4H-1A130_assertion wasDerivedFrom uniprot-20150221 NP3287.RAtBT-nKTHLHM4x8ieWLViB4XgXRJcJ7fZNwQwcz4H-1A130_provenance.
- NP3287.RAtBT-nKTHLHM4x8ieWLViB4XgXRJcJ7fZNwQwcz4H-1A130_assertion wasGeneratedBy ECO_0000218 NP3287.RAtBT-nKTHLHM4x8ieWLViB4XgXRJcJ7fZNwQwcz4H-1A130_provenance.