Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP211.RAfnjf-9gpMkcz_96tN-L__KH0M79cyaZlXcWKTykMjlg130_assertion> ?p ?o ?g. }
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- NP211.RAfnjf-9gpMkcz_96tN-L__KH0M79cyaZlXcWKTykMjlg130_assertion type Assertion NP211.RAfnjf-9gpMkcz_96tN-L__KH0M79cyaZlXcWKTykMjlg130_head.
- NP211.RAfnjf-9gpMkcz_96tN-L__KH0M79cyaZlXcWKTykMjlg130_assertion wasGeneratedBy ECO_0000218 NP211.RAfnjf-9gpMkcz_96tN-L__KH0M79cyaZlXcWKTykMjlg130_provenance.
- NP211.RAfnjf-9gpMkcz_96tN-L__KH0M79cyaZlXcWKTykMjlg130_assertion wasDerivedFrom uniprot-20150221 NP211.RAfnjf-9gpMkcz_96tN-L__KH0M79cyaZlXcWKTykMjlg130_provenance.
- NP211.RAfnjf-9gpMkcz_96tN-L__KH0M79cyaZlXcWKTykMjlg130_assertion SIO_000772 20729831 NP211.RAfnjf-9gpMkcz_96tN-L__KH0M79cyaZlXcWKTykMjlg130_provenance.
- NP211.RAfnjf-9gpMkcz_96tN-L__KH0M79cyaZlXcWKTykMjlg130_assertion evidence source_evidence_curated NP211.RAfnjf-9gpMkcz_96tN-L__KH0M79cyaZlXcWKTykMjlg130_provenance.
- NP211.RAfnjf-9gpMkcz_96tN-L__KH0M79cyaZlXcWKTykMjlg130_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." NP211.RAfnjf-9gpMkcz_96tN-L__KH0M79cyaZlXcWKTykMjlg130_provenance.