Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP261657.RAMq6wbZ4Eixht9-ypVEfkp6bxOWpjAUb2r9M1xdgZyNg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP261657.RAMq6wbZ4Eixht9-ypVEfkp6bxOWpjAUb2r9M1xdgZyNg130_assertion type Assertion NP261657.RAMq6wbZ4Eixht9-ypVEfkp6bxOWpjAUb2r9M1xdgZyNg130_head.
- NP261657.RAMq6wbZ4Eixht9-ypVEfkp6bxOWpjAUb2r9M1xdgZyNg130_assertion description "[As more than 85% of Opitz G/BBB syndrome (OS) patients with MID1 mutations are manifested with hypospadias, we have investigated the association between the MID1 gene and hypospadias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261657.RAMq6wbZ4Eixht9-ypVEfkp6bxOWpjAUb2r9M1xdgZyNg130_provenance.
- NP261657.RAMq6wbZ4Eixht9-ypVEfkp6bxOWpjAUb2r9M1xdgZyNg130_assertion evidence source_evidence_literature NP261657.RAMq6wbZ4Eixht9-ypVEfkp6bxOWpjAUb2r9M1xdgZyNg130_provenance.
- NP261657.RAMq6wbZ4Eixht9-ypVEfkp6bxOWpjAUb2r9M1xdgZyNg130_assertion SIO_000772 21326312 NP261657.RAMq6wbZ4Eixht9-ypVEfkp6bxOWpjAUb2r9M1xdgZyNg130_provenance.
- NP261657.RAMq6wbZ4Eixht9-ypVEfkp6bxOWpjAUb2r9M1xdgZyNg130_assertion wasDerivedFrom befree-20140225 NP261657.RAMq6wbZ4Eixht9-ypVEfkp6bxOWpjAUb2r9M1xdgZyNg130_provenance.
- NP261657.RAMq6wbZ4Eixht9-ypVEfkp6bxOWpjAUb2r9M1xdgZyNg130_assertion wasGeneratedBy ECO_0000203 NP261657.RAMq6wbZ4Eixht9-ypVEfkp6bxOWpjAUb2r9M1xdgZyNg130_provenance.