Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP8086.RAhEvS3UDx9aK3hIlKHxvmB5N3I1FoNHQC-jbTE5eeMGI130_assertion> ?p ?o ?g. }
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- NP8086.RAhEvS3UDx9aK3hIlKHxvmB5N3I1FoNHQC-jbTE5eeMGI130_assertion type Assertion NP8086.RAhEvS3UDx9aK3hIlKHxvmB5N3I1FoNHQC-jbTE5eeMGI130_head.
- NP8086.RAhEvS3UDx9aK3hIlKHxvmB5N3I1FoNHQC-jbTE5eeMGI130_assertion description "[Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8086.RAhEvS3UDx9aK3hIlKHxvmB5N3I1FoNHQC-jbTE5eeMGI130_provenance.
- NP8086.RAhEvS3UDx9aK3hIlKHxvmB5N3I1FoNHQC-jbTE5eeMGI130_assertion evidence source_evidence_curated NP8086.RAhEvS3UDx9aK3hIlKHxvmB5N3I1FoNHQC-jbTE5eeMGI130_provenance.
- NP8086.RAhEvS3UDx9aK3hIlKHxvmB5N3I1FoNHQC-jbTE5eeMGI130_assertion SIO_000772 25480037 NP8086.RAhEvS3UDx9aK3hIlKHxvmB5N3I1FoNHQC-jbTE5eeMGI130_provenance.
- NP8086.RAhEvS3UDx9aK3hIlKHxvmB5N3I1FoNHQC-jbTE5eeMGI130_assertion wasDerivedFrom uniprot-2016 NP8086.RAhEvS3UDx9aK3hIlKHxvmB5N3I1FoNHQC-jbTE5eeMGI130_provenance.
- NP8086.RAhEvS3UDx9aK3hIlKHxvmB5N3I1FoNHQC-jbTE5eeMGI130_assertion wasGeneratedBy ECO_0000218 NP8086.RAhEvS3UDx9aK3hIlKHxvmB5N3I1FoNHQC-jbTE5eeMGI130_provenance.