Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6331.RANJpNYS8C7DGY7yd9voKD0LWCmsFSsuHjk0zudJarG6s130_assertion> ?p ?o ?g. }
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- NP6331.RANJpNYS8C7DGY7yd9voKD0LWCmsFSsuHjk0zudJarG6s130_assertion type Assertion NP6331.RANJpNYS8C7DGY7yd9voKD0LWCmsFSsuHjk0zudJarG6s130_head.
- NP6331.RANJpNYS8C7DGY7yd9voKD0LWCmsFSsuHjk0zudJarG6s130_assertion description "[Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6331.RANJpNYS8C7DGY7yd9voKD0LWCmsFSsuHjk0zudJarG6s130_provenance.
- NP6331.RANJpNYS8C7DGY7yd9voKD0LWCmsFSsuHjk0zudJarG6s130_assertion evidence source_evidence_curated NP6331.RANJpNYS8C7DGY7yd9voKD0LWCmsFSsuHjk0zudJarG6s130_provenance.
- NP6331.RANJpNYS8C7DGY7yd9voKD0LWCmsFSsuHjk0zudJarG6s130_assertion SIO_000772 20729831 NP6331.RANJpNYS8C7DGY7yd9voKD0LWCmsFSsuHjk0zudJarG6s130_provenance.
- NP6331.RANJpNYS8C7DGY7yd9voKD0LWCmsFSsuHjk0zudJarG6s130_assertion wasDerivedFrom uniprot-2016 NP6331.RANJpNYS8C7DGY7yd9voKD0LWCmsFSsuHjk0zudJarG6s130_provenance.
- NP6331.RANJpNYS8C7DGY7yd9voKD0LWCmsFSsuHjk0zudJarG6s130_assertion wasGeneratedBy ECO_0000218 NP6331.RANJpNYS8C7DGY7yd9voKD0LWCmsFSsuHjk0zudJarG6s130_provenance.