Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP498215.RAuyCbbydAYwlQcl0DtPRs_BV6a9QFfUxdmHjYzBFcg_U130_assertion> ?p ?o ?g. }
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- NP498215.RAuyCbbydAYwlQcl0DtPRs_BV6a9QFfUxdmHjYzBFcg_U130_assertion type Assertion NP498215.RAuyCbbydAYwlQcl0DtPRs_BV6a9QFfUxdmHjYzBFcg_U130_head.
- NP498215.RAuyCbbydAYwlQcl0DtPRs_BV6a9QFfUxdmHjYzBFcg_U130_assertion description "[A de novo 4.4-Mb microdeletion in 2p24.3 ? p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498215.RAuyCbbydAYwlQcl0DtPRs_BV6a9QFfUxdmHjYzBFcg_U130_provenance.
- NP498215.RAuyCbbydAYwlQcl0DtPRs_BV6a9QFfUxdmHjYzBFcg_U130_assertion evidence source_evidence_literature NP498215.RAuyCbbydAYwlQcl0DtPRs_BV6a9QFfUxdmHjYzBFcg_U130_provenance.
- NP498215.RAuyCbbydAYwlQcl0DtPRs_BV6a9QFfUxdmHjYzBFcg_U130_assertion SIO_000772 22842076 NP498215.RAuyCbbydAYwlQcl0DtPRs_BV6a9QFfUxdmHjYzBFcg_U130_provenance.
- NP498215.RAuyCbbydAYwlQcl0DtPRs_BV6a9QFfUxdmHjYzBFcg_U130_assertion wasDerivedFrom befree-20140225 NP498215.RAuyCbbydAYwlQcl0DtPRs_BV6a9QFfUxdmHjYzBFcg_U130_provenance.
- NP498215.RAuyCbbydAYwlQcl0DtPRs_BV6a9QFfUxdmHjYzBFcg_U130_assertion wasGeneratedBy ECO_0000203 NP498215.RAuyCbbydAYwlQcl0DtPRs_BV6a9QFfUxdmHjYzBFcg_U130_provenance.