Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP31278.RAMfHqAMtSEhtm1Vl7CXI948o2IN8wPihQ3inoYUx-__s130_assertion> ?p ?o ?g. }
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- NP31278.RAMfHqAMtSEhtm1Vl7CXI948o2IN8wPihQ3inoYUx-__s130_assertion type Assertion NP31278.RAMfHqAMtSEhtm1Vl7CXI948o2IN8wPihQ3inoYUx-__s130_head.
- NP31278.RAMfHqAMtSEhtm1Vl7CXI948o2IN8wPihQ3inoYUx-__s130_assertion description "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31278.RAMfHqAMtSEhtm1Vl7CXI948o2IN8wPihQ3inoYUx-__s130_provenance.
- NP31278.RAMfHqAMtSEhtm1Vl7CXI948o2IN8wPihQ3inoYUx-__s130_assertion evidence source_evidence_curated NP31278.RAMfHqAMtSEhtm1Vl7CXI948o2IN8wPihQ3inoYUx-__s130_provenance.
- NP31278.RAMfHqAMtSEhtm1Vl7CXI948o2IN8wPihQ3inoYUx-__s130_assertion SIO_000772 22544363 NP31278.RAMfHqAMtSEhtm1Vl7CXI948o2IN8wPihQ3inoYUx-__s130_provenance.
- NP31278.RAMfHqAMtSEhtm1Vl7CXI948o2IN8wPihQ3inoYUx-__s130_assertion wasDerivedFrom ctd_human-2016 NP31278.RAMfHqAMtSEhtm1Vl7CXI948o2IN8wPihQ3inoYUx-__s130_provenance.
- NP31278.RAMfHqAMtSEhtm1Vl7CXI948o2IN8wPihQ3inoYUx-__s130_assertion wasGeneratedBy ECO_0000218 NP31278.RAMfHqAMtSEhtm1Vl7CXI948o2IN8wPihQ3inoYUx-__s130_provenance.