Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP530468.RApwdrThZq4Jaq0fT-NmHrtRt74F0GxA6daDhitSSJB98130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP530468.RApwdrThZq4Jaq0fT-NmHrtRt74F0GxA6daDhitSSJB98130_assertion type Assertion NP530468.RApwdrThZq4Jaq0fT-NmHrtRt74F0GxA6daDhitSSJB98130_head.
- NP530468.RApwdrThZq4Jaq0fT-NmHrtRt74F0GxA6daDhitSSJB98130_assertion wasGeneratedBy ECO_0000203 NP530468.RApwdrThZq4Jaq0fT-NmHrtRt74F0GxA6daDhitSSJB98130_provenance.
- NP530468.RApwdrThZq4Jaq0fT-NmHrtRt74F0GxA6daDhitSSJB98130_assertion wasDerivedFrom befree-20150227 NP530468.RApwdrThZq4Jaq0fT-NmHrtRt74F0GxA6daDhitSSJB98130_provenance.
- NP530468.RApwdrThZq4Jaq0fT-NmHrtRt74F0GxA6daDhitSSJB98130_assertion SIO_000772 21236492 NP530468.RApwdrThZq4Jaq0fT-NmHrtRt74F0GxA6daDhitSSJB98130_provenance.
- NP530468.RApwdrThZq4Jaq0fT-NmHrtRt74F0GxA6daDhitSSJB98130_assertion evidence source_evidence_literature NP530468.RApwdrThZq4Jaq0fT-NmHrtRt74F0GxA6daDhitSSJB98130_provenance.
- NP530468.RApwdrThZq4Jaq0fT-NmHrtRt74F0GxA6daDhitSSJB98130_assertion description "[To describe a novel laminin β-2 (LAMB2) mutation associated with nephrotic syndrome and severe retinal disease without microcoria in a large, multigenerational family with Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530468.RApwdrThZq4Jaq0fT-NmHrtRt74F0GxA6daDhitSSJB98130_provenance.