Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP592626.RA4FlKHiNMpdipNs0mJ_1N7LUT3DxB5JCz0zKxNAWK1-8130_assertion> ?p ?o ?g. }
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- NP592626.RA4FlKHiNMpdipNs0mJ_1N7LUT3DxB5JCz0zKxNAWK1-8130_assertion type Assertion NP592626.RA4FlKHiNMpdipNs0mJ_1N7LUT3DxB5JCz0zKxNAWK1-8130_head.
- NP592626.RA4FlKHiNMpdipNs0mJ_1N7LUT3DxB5JCz0zKxNAWK1-8130_assertion description "[Deletion 11(p11.2p12) is a rare, yet specific, deletion syndrome involving the EXT2 locus, a gene for parietal foramina, and a mental retardation locus, and therefore can be classified as a contiguous gene deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592626.RA4FlKHiNMpdipNs0mJ_1N7LUT3DxB5JCz0zKxNAWK1-8130_provenance.
- NP592626.RA4FlKHiNMpdipNs0mJ_1N7LUT3DxB5JCz0zKxNAWK1-8130_assertion evidence source_evidence_literature NP592626.RA4FlKHiNMpdipNs0mJ_1N7LUT3DxB5JCz0zKxNAWK1-8130_provenance.
- NP592626.RA4FlKHiNMpdipNs0mJ_1N7LUT3DxB5JCz0zKxNAWK1-8130_assertion SIO_000772 8882796 NP592626.RA4FlKHiNMpdipNs0mJ_1N7LUT3DxB5JCz0zKxNAWK1-8130_provenance.
- NP592626.RA4FlKHiNMpdipNs0mJ_1N7LUT3DxB5JCz0zKxNAWK1-8130_assertion wasDerivedFrom befree-20140225 NP592626.RA4FlKHiNMpdipNs0mJ_1N7LUT3DxB5JCz0zKxNAWK1-8130_provenance.
- NP592626.RA4FlKHiNMpdipNs0mJ_1N7LUT3DxB5JCz0zKxNAWK1-8130_assertion wasGeneratedBy ECO_0000203 NP592626.RA4FlKHiNMpdipNs0mJ_1N7LUT3DxB5JCz0zKxNAWK1-8130_provenance.