Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP831116.RA4sFxgNKhWghUkMEJDRbBguiN6jUL9FinMEyIYmsybkw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP831116.RA4sFxgNKhWghUkMEJDRbBguiN6jUL9FinMEyIYmsybkw130_assertion type Assertion NP831116.RA4sFxgNKhWghUkMEJDRbBguiN6jUL9FinMEyIYmsybkw130_head.
- NP831116.RA4sFxgNKhWghUkMEJDRbBguiN6jUL9FinMEyIYmsybkw130_assertion description "[These results allow further delineation of the spectrum of malformations ascribed to SMADIP1 haploinsufficiency, which includes frequent features such as hypospadias and agenesis of the corpus callosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831116.RA4sFxgNKhWghUkMEJDRbBguiN6jUL9FinMEyIYmsybkw130_provenance.
- NP831116.RA4sFxgNKhWghUkMEJDRbBguiN6jUL9FinMEyIYmsybkw130_assertion evidence source_evidence_literature NP831116.RA4sFxgNKhWghUkMEJDRbBguiN6jUL9FinMEyIYmsybkw130_provenance.
- NP831116.RA4sFxgNKhWghUkMEJDRbBguiN6jUL9FinMEyIYmsybkw130_assertion SIO_000772 11595972 NP831116.RA4sFxgNKhWghUkMEJDRbBguiN6jUL9FinMEyIYmsybkw130_provenance.
- NP831116.RA4sFxgNKhWghUkMEJDRbBguiN6jUL9FinMEyIYmsybkw130_assertion wasDerivedFrom befree-20150227 NP831116.RA4sFxgNKhWghUkMEJDRbBguiN6jUL9FinMEyIYmsybkw130_provenance.
- NP831116.RA4sFxgNKhWghUkMEJDRbBguiN6jUL9FinMEyIYmsybkw130_assertion wasGeneratedBy ECO_0000203 NP831116.RA4sFxgNKhWghUkMEJDRbBguiN6jUL9FinMEyIYmsybkw130_provenance.