Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1152.RAneQl78v1j9ZhkWwHdD1AoombCsFJ1uo6RfyYVYoN6Gc130_assertion> ?p ?o ?g. }
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- NP1152.RAneQl78v1j9ZhkWwHdD1AoombCsFJ1uo6RfyYVYoN6Gc130_assertion type Assertion NP1152.RAneQl78v1j9ZhkWwHdD1AoombCsFJ1uo6RfyYVYoN6Gc130_head.
- NP1152.RAneQl78v1j9ZhkWwHdD1AoombCsFJ1uo6RfyYVYoN6Gc130_assertion description "[The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1152.RAneQl78v1j9ZhkWwHdD1AoombCsFJ1uo6RfyYVYoN6Gc130_provenance.
- NP1152.RAneQl78v1j9ZhkWwHdD1AoombCsFJ1uo6RfyYVYoN6Gc130_assertion evidence source_evidence_curated NP1152.RAneQl78v1j9ZhkWwHdD1AoombCsFJ1uo6RfyYVYoN6Gc130_provenance.
- NP1152.RAneQl78v1j9ZhkWwHdD1AoombCsFJ1uo6RfyYVYoN6Gc130_assertion SIO_000772 11106354 NP1152.RAneQl78v1j9ZhkWwHdD1AoombCsFJ1uo6RfyYVYoN6Gc130_provenance.
- NP1152.RAneQl78v1j9ZhkWwHdD1AoombCsFJ1uo6RfyYVYoN6Gc130_assertion wasDerivedFrom uniprot-2016 NP1152.RAneQl78v1j9ZhkWwHdD1AoombCsFJ1uo6RfyYVYoN6Gc130_provenance.
- NP1152.RAneQl78v1j9ZhkWwHdD1AoombCsFJ1uo6RfyYVYoN6Gc130_assertion wasGeneratedBy ECO_0000218 NP1152.RAneQl78v1j9ZhkWwHdD1AoombCsFJ1uo6RfyYVYoN6Gc130_provenance.