Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP530558.RAef3LULpwIj8s7qrEepD09ZIS-DSRgMWuIorrH21A9EE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP530558.RAef3LULpwIj8s7qrEepD09ZIS-DSRgMWuIorrH21A9EE130_assertion type Assertion NP530558.RAef3LULpwIj8s7qrEepD09ZIS-DSRgMWuIorrH21A9EE130_head.
- NP530558.RAef3LULpwIj8s7qrEepD09ZIS-DSRgMWuIorrH21A9EE130_assertion wasGeneratedBy ECO_0000203 NP530558.RAef3LULpwIj8s7qrEepD09ZIS-DSRgMWuIorrH21A9EE130_provenance.
- NP530558.RAef3LULpwIj8s7qrEepD09ZIS-DSRgMWuIorrH21A9EE130_assertion wasDerivedFrom befree-20150227 NP530558.RAef3LULpwIj8s7qrEepD09ZIS-DSRgMWuIorrH21A9EE130_provenance.
- NP530558.RAef3LULpwIj8s7qrEepD09ZIS-DSRgMWuIorrH21A9EE130_assertion SIO_000772 21236492 NP530558.RAef3LULpwIj8s7qrEepD09ZIS-DSRgMWuIorrH21A9EE130_provenance.
- NP530558.RAef3LULpwIj8s7qrEepD09ZIS-DSRgMWuIorrH21A9EE130_assertion evidence source_evidence_literature NP530558.RAef3LULpwIj8s7qrEepD09ZIS-DSRgMWuIorrH21A9EE130_provenance.
- NP530558.RAef3LULpwIj8s7qrEepD09ZIS-DSRgMWuIorrH21A9EE130_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." NP530558.RAef3LULpwIj8s7qrEepD09ZIS-DSRgMWuIorrH21A9EE130_provenance.