Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP133062.RAFFUZ05ltl0f4pgZ8DmCmy0zIaRv80H0n81gSIMXVcUU130_assertion> ?p ?o ?g. }
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- NP133062.RAFFUZ05ltl0f4pgZ8DmCmy0zIaRv80H0n81gSIMXVcUU130_assertion type Assertion NP133062.RAFFUZ05ltl0f4pgZ8DmCmy0zIaRv80H0n81gSIMXVcUU130_head.
- NP133062.RAFFUZ05ltl0f4pgZ8DmCmy0zIaRv80H0n81gSIMXVcUU130_assertion wasGeneratedBy ECO_0000203 NP133062.RAFFUZ05ltl0f4pgZ8DmCmy0zIaRv80H0n81gSIMXVcUU130_provenance.
- NP133062.RAFFUZ05ltl0f4pgZ8DmCmy0zIaRv80H0n81gSIMXVcUU130_assertion wasDerivedFrom lhgdn-20090331 NP133062.RAFFUZ05ltl0f4pgZ8DmCmy0zIaRv80H0n81gSIMXVcUU130_provenance.
- NP133062.RAFFUZ05ltl0f4pgZ8DmCmy0zIaRv80H0n81gSIMXVcUU130_assertion SIO_000772 18405873 NP133062.RAFFUZ05ltl0f4pgZ8DmCmy0zIaRv80H0n81gSIMXVcUU130_provenance.
- NP133062.RAFFUZ05ltl0f4pgZ8DmCmy0zIaRv80H0n81gSIMXVcUU130_assertion evidence source_evidence_literature NP133062.RAFFUZ05ltl0f4pgZ8DmCmy0zIaRv80H0n81gSIMXVcUU130_provenance.
- NP133062.RAFFUZ05ltl0f4pgZ8DmCmy0zIaRv80H0n81gSIMXVcUU130_assertion description "[truncating mutations of DYRK1A result in a clinical phenotype including microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133062.RAFFUZ05ltl0f4pgZ8DmCmy0zIaRv80H0n81gSIMXVcUU130_provenance.