Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP822309.RAfEnMOb-QK92cPm12EVgxFDSRUFM1--2bhD5uoZm5QLs130_assertion> ?p ?o ?g. }
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- NP822309.RAfEnMOb-QK92cPm12EVgxFDSRUFM1--2bhD5uoZm5QLs130_assertion type Assertion NP822309.RAfEnMOb-QK92cPm12EVgxFDSRUFM1--2bhD5uoZm5QLs130_head.
- NP822309.RAfEnMOb-QK92cPm12EVgxFDSRUFM1--2bhD5uoZm5QLs130_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." NP822309.RAfEnMOb-QK92cPm12EVgxFDSRUFM1--2bhD5uoZm5QLs130_provenance.
- NP822309.RAfEnMOb-QK92cPm12EVgxFDSRUFM1--2bhD5uoZm5QLs130_assertion evidence source_evidence_literature NP822309.RAfEnMOb-QK92cPm12EVgxFDSRUFM1--2bhD5uoZm5QLs130_provenance.
- NP822309.RAfEnMOb-QK92cPm12EVgxFDSRUFM1--2bhD5uoZm5QLs130_assertion SIO_000772 8882796 NP822309.RAfEnMOb-QK92cPm12EVgxFDSRUFM1--2bhD5uoZm5QLs130_provenance.
- NP822309.RAfEnMOb-QK92cPm12EVgxFDSRUFM1--2bhD5uoZm5QLs130_assertion wasDerivedFrom befree-20140225 NP822309.RAfEnMOb-QK92cPm12EVgxFDSRUFM1--2bhD5uoZm5QLs130_provenance.
- NP822309.RAfEnMOb-QK92cPm12EVgxFDSRUFM1--2bhD5uoZm5QLs130_assertion wasGeneratedBy ECO_0000203 NP822309.RAfEnMOb-QK92cPm12EVgxFDSRUFM1--2bhD5uoZm5QLs130_provenance.