Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP10026.RAFvG-Wm4qvUXIYZF9EITWckrQ1S5yxTgJ3UytD9S9aZQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP10026.RAFvG-Wm4qvUXIYZF9EITWckrQ1S5yxTgJ3UytD9S9aZQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP10026.RAFvG-Wm4qvUXIYZF9EITWckrQ1S5yxTgJ3UytD9S9aZQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP10026.RAFvG-Wm4qvUXIYZF9EITWckrQ1S5yxTgJ3UytD9S9aZQ130_provenance.
- NP10026.RAFvG-Wm4qvUXIYZF9EITWckrQ1S5yxTgJ3UytD9S9aZQ130_assertion description "[Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10026.RAFvG-Wm4qvUXIYZF9EITWckrQ1S5yxTgJ3UytD9S9aZQ130_provenance.
- NP10026.RAFvG-Wm4qvUXIYZF9EITWckrQ1S5yxTgJ3UytD9S9aZQ130_assertion evidence source_evidence_curated NP10026.RAFvG-Wm4qvUXIYZF9EITWckrQ1S5yxTgJ3UytD9S9aZQ130_provenance.
- NP10026.RAFvG-Wm4qvUXIYZF9EITWckrQ1S5yxTgJ3UytD9S9aZQ130_assertion SIO_000772 9916847 NP10026.RAFvG-Wm4qvUXIYZF9EITWckrQ1S5yxTgJ3UytD9S9aZQ130_provenance.
- NP10026.RAFvG-Wm4qvUXIYZF9EITWckrQ1S5yxTgJ3UytD9S9aZQ130_assertion wasDerivedFrom uniprot-2016 NP10026.RAFvG-Wm4qvUXIYZF9EITWckrQ1S5yxTgJ3UytD9S9aZQ130_provenance.
- NP10026.RAFvG-Wm4qvUXIYZF9EITWckrQ1S5yxTgJ3UytD9S9aZQ130_assertion wasGeneratedBy ECO_0000218 NP10026.RAFvG-Wm4qvUXIYZF9EITWckrQ1S5yxTgJ3UytD9S9aZQ130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP10026.RAFvG-Wm4qvUXIYZF9EITWckrQ1S5yxTgJ3UytD9S9aZQ130_provenance.