Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_assertion> ?p ?o ?g. }
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- NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_assertion type Assertion NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_head.
- NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_assertion description "[De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_provenance.
- NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_assertion evidence source_evidence_literature NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_provenance.
- NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_assertion SIO_000772 21706002 NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_provenance.
- NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_assertion wasDerivedFrom befree-20140225 NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_provenance.
- NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_assertion wasGeneratedBy ECO_0000203 NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_provenance.