Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP197185.RAbAkUB0Sl-J9VMlvWzbCJ3DkCBjgpoqIE0Gyf69iROsc130_assertion> ?p ?o ?g. }
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- NP197185.RAbAkUB0Sl-J9VMlvWzbCJ3DkCBjgpoqIE0Gyf69iROsc130_assertion type Assertion NP197185.RAbAkUB0Sl-J9VMlvWzbCJ3DkCBjgpoqIE0Gyf69iROsc130_head.
- NP197185.RAbAkUB0Sl-J9VMlvWzbCJ3DkCBjgpoqIE0Gyf69iROsc130_assertion wasGeneratedBy ECO_0000203 NP197185.RAbAkUB0Sl-J9VMlvWzbCJ3DkCBjgpoqIE0Gyf69iROsc130_provenance.
- NP197185.RAbAkUB0Sl-J9VMlvWzbCJ3DkCBjgpoqIE0Gyf69iROsc130_assertion wasDerivedFrom lhgdn-20090331 NP197185.RAbAkUB0Sl-J9VMlvWzbCJ3DkCBjgpoqIE0Gyf69iROsc130_provenance.
- NP197185.RAbAkUB0Sl-J9VMlvWzbCJ3DkCBjgpoqIE0Gyf69iROsc130_assertion SIO_000772 12459588 NP197185.RAbAkUB0Sl-J9VMlvWzbCJ3DkCBjgpoqIE0Gyf69iROsc130_provenance.
- NP197185.RAbAkUB0Sl-J9VMlvWzbCJ3DkCBjgpoqIE0Gyf69iROsc130_assertion evidence source_evidence_literature NP197185.RAbAkUB0Sl-J9VMlvWzbCJ3DkCBjgpoqIE0Gyf69iROsc130_provenance.
- NP197185.RAbAkUB0Sl-J9VMlvWzbCJ3DkCBjgpoqIE0Gyf69iROsc130_assertion description "[4-base pair deletion in the neurotrypsin gene was associated with autosomal recessive nonsyndromic mental retardation; findings suggest that neurotrypsin-mediated proteolysis is required for normal synaptic function ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197185.RAbAkUB0Sl-J9VMlvWzbCJ3DkCBjgpoqIE0Gyf69iROsc130_provenance.