Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7631.RATUq_Z8fEQ5FSttsDoUhOKYp8QdIFCfvScuHEHrhS-NE130_assertion> ?p ?o ?g. }
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- NP7631.RATUq_Z8fEQ5FSttsDoUhOKYp8QdIFCfvScuHEHrhS-NE130_assertion type Assertion NP7631.RATUq_Z8fEQ5FSttsDoUhOKYp8QdIFCfvScuHEHrhS-NE130_head.
- NP7631.RATUq_Z8fEQ5FSttsDoUhOKYp8QdIFCfvScuHEHrhS-NE130_assertion description "[BMP9 mutations cause a vascular-anomaly syndrome with phenotypic overlap with hereditary hemorrhagic telangiectasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7631.RATUq_Z8fEQ5FSttsDoUhOKYp8QdIFCfvScuHEHrhS-NE130_provenance.
- NP7631.RATUq_Z8fEQ5FSttsDoUhOKYp8QdIFCfvScuHEHrhS-NE130_assertion evidence source_evidence_curated NP7631.RATUq_Z8fEQ5FSttsDoUhOKYp8QdIFCfvScuHEHrhS-NE130_provenance.
- NP7631.RATUq_Z8fEQ5FSttsDoUhOKYp8QdIFCfvScuHEHrhS-NE130_assertion SIO_000772 23972370 NP7631.RATUq_Z8fEQ5FSttsDoUhOKYp8QdIFCfvScuHEHrhS-NE130_provenance.
- NP7631.RATUq_Z8fEQ5FSttsDoUhOKYp8QdIFCfvScuHEHrhS-NE130_assertion wasDerivedFrom uniprot-2016 NP7631.RATUq_Z8fEQ5FSttsDoUhOKYp8QdIFCfvScuHEHrhS-NE130_provenance.
- NP7631.RATUq_Z8fEQ5FSttsDoUhOKYp8QdIFCfvScuHEHrhS-NE130_assertion wasGeneratedBy ECO_0000218 NP7631.RATUq_Z8fEQ5FSttsDoUhOKYp8QdIFCfvScuHEHrhS-NE130_provenance.