Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_assertion type Assertion NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_head.
- NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_assertion description "[We report on two related individuals who have multiple anomalies with parietal foramina and the deletion of 11(p11.12p12) due to the inheritance of a derivative chromosome 11 from an insertional translocation dir ins (13;11)(q14.1; p11.12p12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_provenance.
- NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_assertion evidence source_evidence_literature NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_provenance.
- NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_assertion SIO_000772 8456828 NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_provenance.
- NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_assertion wasDerivedFrom befree-20140225 NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_provenance.
- NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_assertion wasGeneratedBy ECO_0000203 NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_provenance.