Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP800410.RADYA2Gp3lYgpodSGxi0x7Nc5sk4xWE9OtCAca0rQojB8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP800410.RADYA2Gp3lYgpodSGxi0x7Nc5sk4xWE9OtCAca0rQojB8130_assertion type Assertion NP800410.RADYA2Gp3lYgpodSGxi0x7Nc5sk4xWE9OtCAca0rQojB8130_head.
- NP800410.RADYA2Gp3lYgpodSGxi0x7Nc5sk4xWE9OtCAca0rQojB8130_assertion description "[Genomic organisation of the human chordin gene and mutation screening of candidate Cornelia de Lange syndrome genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800410.RADYA2Gp3lYgpodSGxi0x7Nc5sk4xWE9OtCAca0rQojB8130_provenance.
- NP800410.RADYA2Gp3lYgpodSGxi0x7Nc5sk4xWE9OtCAca0rQojB8130_assertion evidence source_evidence_literature NP800410.RADYA2Gp3lYgpodSGxi0x7Nc5sk4xWE9OtCAca0rQojB8130_provenance.
- NP800410.RADYA2Gp3lYgpodSGxi0x7Nc5sk4xWE9OtCAca0rQojB8130_assertion SIO_000772 10480362 NP800410.RADYA2Gp3lYgpodSGxi0x7Nc5sk4xWE9OtCAca0rQojB8130_provenance.
- NP800410.RADYA2Gp3lYgpodSGxi0x7Nc5sk4xWE9OtCAca0rQojB8130_assertion wasDerivedFrom befree-20150227 NP800410.RADYA2Gp3lYgpodSGxi0x7Nc5sk4xWE9OtCAca0rQojB8130_provenance.
- NP800410.RADYA2Gp3lYgpodSGxi0x7Nc5sk4xWE9OtCAca0rQojB8130_assertion wasGeneratedBy ECO_0000203 NP800410.RADYA2Gp3lYgpodSGxi0x7Nc5sk4xWE9OtCAca0rQojB8130_provenance.