Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1311282.RAHd0XJGvUCZLJ0zXmeXKFbSob0aYjnGxwDMI-XS_BU2w130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1311282.RAHd0XJGvUCZLJ0zXmeXKFbSob0aYjnGxwDMI-XS_BU2w130_assertion type Assertion NP1311282.RAHd0XJGvUCZLJ0zXmeXKFbSob0aYjnGxwDMI-XS_BU2w130_head.
- NP1311282.RAHd0XJGvUCZLJ0zXmeXKFbSob0aYjnGxwDMI-XS_BU2w130_assertion description "[Overlapping submicroscopic deletions in Xq28 in two unrelated boys with developmental disorders: identification of a gene near FRAXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1311282.RAHd0XJGvUCZLJ0zXmeXKFbSob0aYjnGxwDMI-XS_BU2w130_provenance.
- NP1311282.RAHd0XJGvUCZLJ0zXmeXKFbSob0aYjnGxwDMI-XS_BU2w130_assertion evidence source_evidence_literature NP1311282.RAHd0XJGvUCZLJ0zXmeXKFbSob0aYjnGxwDMI-XS_BU2w130_provenance.
- NP1311282.RAHd0XJGvUCZLJ0zXmeXKFbSob0aYjnGxwDMI-XS_BU2w130_assertion SIO_000772 7536393 NP1311282.RAHd0XJGvUCZLJ0zXmeXKFbSob0aYjnGxwDMI-XS_BU2w130_provenance.
- NP1311282.RAHd0XJGvUCZLJ0zXmeXKFbSob0aYjnGxwDMI-XS_BU2w130_assertion wasDerivedFrom befree-2016 NP1311282.RAHd0XJGvUCZLJ0zXmeXKFbSob0aYjnGxwDMI-XS_BU2w130_provenance.
- NP1311282.RAHd0XJGvUCZLJ0zXmeXKFbSob0aYjnGxwDMI-XS_BU2w130_assertion wasGeneratedBy ECO_0000203 NP1311282.RAHd0XJGvUCZLJ0zXmeXKFbSob0aYjnGxwDMI-XS_BU2w130_provenance.