Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP20044.RAwqBp2XHJiR5zNg576ISxRU9C9jOoEdWoV2-HbL5MoHo130_assertion> ?p ?o ?g. }
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- NP20044.RAwqBp2XHJiR5zNg576ISxRU9C9jOoEdWoV2-HbL5MoHo130_assertion type Assertion NP20044.RAwqBp2XHJiR5zNg576ISxRU9C9jOoEdWoV2-HbL5MoHo130_head.
- NP20044.RAwqBp2XHJiR5zNg576ISxRU9C9jOoEdWoV2-HbL5MoHo130_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." NP20044.RAwqBp2XHJiR5zNg576ISxRU9C9jOoEdWoV2-HbL5MoHo130_provenance.
- NP20044.RAwqBp2XHJiR5zNg576ISxRU9C9jOoEdWoV2-HbL5MoHo130_assertion evidence source_evidence_curated NP20044.RAwqBp2XHJiR5zNg576ISxRU9C9jOoEdWoV2-HbL5MoHo130_provenance.
- NP20044.RAwqBp2XHJiR5zNg576ISxRU9C9jOoEdWoV2-HbL5MoHo130_assertion SIO_000772 22544363 NP20044.RAwqBp2XHJiR5zNg576ISxRU9C9jOoEdWoV2-HbL5MoHo130_provenance.
- NP20044.RAwqBp2XHJiR5zNg576ISxRU9C9jOoEdWoV2-HbL5MoHo130_assertion wasDerivedFrom ctd_human-20150221 NP20044.RAwqBp2XHJiR5zNg576ISxRU9C9jOoEdWoV2-HbL5MoHo130_provenance.
- NP20044.RAwqBp2XHJiR5zNg576ISxRU9C9jOoEdWoV2-HbL5MoHo130_assertion wasGeneratedBy ECO_0000218 NP20044.RAwqBp2XHJiR5zNg576ISxRU9C9jOoEdWoV2-HbL5MoHo130_provenance.