Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP9110.RAEK_ro2IxySrTwhn1FTHDXmj11tN2A8b5BhVtB2VWPUc130_assertion> ?p ?o ?g. }
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- NP9110.RAEK_ro2IxySrTwhn1FTHDXmj11tN2A8b5BhVtB2VWPUc130_assertion type Assertion NP9110.RAEK_ro2IxySrTwhn1FTHDXmj11tN2A8b5BhVtB2VWPUc130_head.
- NP9110.RAEK_ro2IxySrTwhn1FTHDXmj11tN2A8b5BhVtB2VWPUc130_assertion description "[A genotype-first approach for the molecular and clinical characterization of uncommon de novo microdeletion of 20q13.33.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9110.RAEK_ro2IxySrTwhn1FTHDXmj11tN2A8b5BhVtB2VWPUc130_provenance.
- NP9110.RAEK_ro2IxySrTwhn1FTHDXmj11tN2A8b5BhVtB2VWPUc130_assertion evidence source_evidence_curated NP9110.RAEK_ro2IxySrTwhn1FTHDXmj11tN2A8b5BhVtB2VWPUc130_provenance.
- NP9110.RAEK_ro2IxySrTwhn1FTHDXmj11tN2A8b5BhVtB2VWPUc130_assertion SIO_000772 20805988 NP9110.RAEK_ro2IxySrTwhn1FTHDXmj11tN2A8b5BhVtB2VWPUc130_provenance.
- NP9110.RAEK_ro2IxySrTwhn1FTHDXmj11tN2A8b5BhVtB2VWPUc130_assertion wasDerivedFrom ctd_human-20130708 NP9110.RAEK_ro2IxySrTwhn1FTHDXmj11tN2A8b5BhVtB2VWPUc130_provenance.
- NP9110.RAEK_ro2IxySrTwhn1FTHDXmj11tN2A8b5BhVtB2VWPUc130_assertion wasGeneratedBy ECO_0000218 NP9110.RAEK_ro2IxySrTwhn1FTHDXmj11tN2A8b5BhVtB2VWPUc130_provenance.