Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP827932.RAmh9IR2RBjqq7x6nDxmZ_9fnFsY_Qwl2Jk7bR3K3ifLY130_assertion> ?p ?o ?g. }
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- NP827932.RAmh9IR2RBjqq7x6nDxmZ_9fnFsY_Qwl2Jk7bR3K3ifLY130_assertion type Assertion NP827932.RAmh9IR2RBjqq7x6nDxmZ_9fnFsY_Qwl2Jk7bR3K3ifLY130_head.
- NP827932.RAmh9IR2RBjqq7x6nDxmZ_9fnFsY_Qwl2Jk7bR3K3ifLY130_assertion description "[Two of the ASD individuals with missense changes also carried a de novo deletion at another ASD susceptibility locus (DPYD and DPP6), suggesting complex genetic contributions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827932.RAmh9IR2RBjqq7x6nDxmZ_9fnFsY_Qwl2Jk7bR3K3ifLY130_provenance.
- NP827932.RAmh9IR2RBjqq7x6nDxmZ_9fnFsY_Qwl2Jk7bR3K3ifLY130_assertion evidence source_evidence_literature NP827932.RAmh9IR2RBjqq7x6nDxmZ_9fnFsY_Qwl2Jk7bR3K3ifLY130_provenance.
- NP827932.RAmh9IR2RBjqq7x6nDxmZ_9fnFsY_Qwl2Jk7bR3K3ifLY130_assertion SIO_000772 20844286 NP827932.RAmh9IR2RBjqq7x6nDxmZ_9fnFsY_Qwl2Jk7bR3K3ifLY130_provenance.
- NP827932.RAmh9IR2RBjqq7x6nDxmZ_9fnFsY_Qwl2Jk7bR3K3ifLY130_assertion wasDerivedFrom befree-20140225 NP827932.RAmh9IR2RBjqq7x6nDxmZ_9fnFsY_Qwl2Jk7bR3K3ifLY130_provenance.
- NP827932.RAmh9IR2RBjqq7x6nDxmZ_9fnFsY_Qwl2Jk7bR3K3ifLY130_assertion wasGeneratedBy ECO_0000203 NP827932.RAmh9IR2RBjqq7x6nDxmZ_9fnFsY_Qwl2Jk7bR3K3ifLY130_provenance.