Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP306758.RAuflzP3Eue1tmp3fUY3zoPFEYH8Ze2IkwfpRAkumNZOw130_assertion> ?p ?o ?g. }
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- NP306758.RAuflzP3Eue1tmp3fUY3zoPFEYH8Ze2IkwfpRAkumNZOw130_assertion type Assertion NP306758.RAuflzP3Eue1tmp3fUY3zoPFEYH8Ze2IkwfpRAkumNZOw130_head.
- NP306758.RAuflzP3Eue1tmp3fUY3zoPFEYH8Ze2IkwfpRAkumNZOw130_assertion wasGeneratedBy ECO_0000203 NP306758.RAuflzP3Eue1tmp3fUY3zoPFEYH8Ze2IkwfpRAkumNZOw130_provenance.
- NP306758.RAuflzP3Eue1tmp3fUY3zoPFEYH8Ze2IkwfpRAkumNZOw130_assertion wasDerivedFrom befree-20140225 NP306758.RAuflzP3Eue1tmp3fUY3zoPFEYH8Ze2IkwfpRAkumNZOw130_provenance.
- NP306758.RAuflzP3Eue1tmp3fUY3zoPFEYH8Ze2IkwfpRAkumNZOw130_assertion SIO_000772 23527149 NP306758.RAuflzP3Eue1tmp3fUY3zoPFEYH8Ze2IkwfpRAkumNZOw130_provenance.
- NP306758.RAuflzP3Eue1tmp3fUY3zoPFEYH8Ze2IkwfpRAkumNZOw130_assertion evidence source_evidence_literature NP306758.RAuflzP3Eue1tmp3fUY3zoPFEYH8Ze2IkwfpRAkumNZOw130_provenance.
- NP306758.RAuflzP3Eue1tmp3fUY3zoPFEYH8Ze2IkwfpRAkumNZOw130_assertion description "[Fine mapping for Weaver syndrome in Brown Swiss cattle and the identification of 41 concordant mutations across NRCAM, PNPLA8 and CTTNBP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP306758.RAuflzP3Eue1tmp3fUY3zoPFEYH8Ze2IkwfpRAkumNZOw130_provenance.