Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP610936.RAK9uQuN4Iexfg6DOX5Uebpmp9OxB0E9sLPPiXvARSlnQ130_assertion> ?p ?o ?g. }
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- NP610936.RAK9uQuN4Iexfg6DOX5Uebpmp9OxB0E9sLPPiXvARSlnQ130_assertion type Assertion NP610936.RAK9uQuN4Iexfg6DOX5Uebpmp9OxB0E9sLPPiXvARSlnQ130_head.
- NP610936.RAK9uQuN4Iexfg6DOX5Uebpmp9OxB0E9sLPPiXvARSlnQ130_assertion wasGeneratedBy ECO_0000203 NP610936.RAK9uQuN4Iexfg6DOX5Uebpmp9OxB0E9sLPPiXvARSlnQ130_provenance.
- NP610936.RAK9uQuN4Iexfg6DOX5Uebpmp9OxB0E9sLPPiXvARSlnQ130_assertion wasDerivedFrom befree-20140225 NP610936.RAK9uQuN4Iexfg6DOX5Uebpmp9OxB0E9sLPPiXvARSlnQ130_provenance.
- NP610936.RAK9uQuN4Iexfg6DOX5Uebpmp9OxB0E9sLPPiXvARSlnQ130_assertion SIO_000772 21326312 NP610936.RAK9uQuN4Iexfg6DOX5Uebpmp9OxB0E9sLPPiXvARSlnQ130_provenance.
- NP610936.RAK9uQuN4Iexfg6DOX5Uebpmp9OxB0E9sLPPiXvARSlnQ130_assertion evidence source_evidence_literature NP610936.RAK9uQuN4Iexfg6DOX5Uebpmp9OxB0E9sLPPiXvARSlnQ130_provenance.
- NP610936.RAK9uQuN4Iexfg6DOX5Uebpmp9OxB0E9sLPPiXvARSlnQ130_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." NP610936.RAK9uQuN4Iexfg6DOX5Uebpmp9OxB0E9sLPPiXvARSlnQ130_provenance.