Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6488.RA0WHQGMDQ3IhTUlElkPioAJodNUil6EFeRrngoPFhL2g130_assertion> ?p ?o ?g. }
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- NP6488.RA0WHQGMDQ3IhTUlElkPioAJodNUil6EFeRrngoPFhL2g130_assertion type Assertion NP6488.RA0WHQGMDQ3IhTUlElkPioAJodNUil6EFeRrngoPFhL2g130_head.
- NP6488.RA0WHQGMDQ3IhTUlElkPioAJodNUil6EFeRrngoPFhL2g130_assertion wasGeneratedBy ECO_0000218 NP6488.RA0WHQGMDQ3IhTUlElkPioAJodNUil6EFeRrngoPFhL2g130_provenance.
- NP6488.RA0WHQGMDQ3IhTUlElkPioAJodNUil6EFeRrngoPFhL2g130_assertion wasDerivedFrom uniprot-2016 NP6488.RA0WHQGMDQ3IhTUlElkPioAJodNUil6EFeRrngoPFhL2g130_provenance.
- NP6488.RA0WHQGMDQ3IhTUlElkPioAJodNUil6EFeRrngoPFhL2g130_assertion SIO_000772 21236492 NP6488.RA0WHQGMDQ3IhTUlElkPioAJodNUil6EFeRrngoPFhL2g130_provenance.
- NP6488.RA0WHQGMDQ3IhTUlElkPioAJodNUil6EFeRrngoPFhL2g130_assertion evidence source_evidence_curated NP6488.RA0WHQGMDQ3IhTUlElkPioAJodNUil6EFeRrngoPFhL2g130_provenance.
- NP6488.RA0WHQGMDQ3IhTUlElkPioAJodNUil6EFeRrngoPFhL2g130_assertion description "[A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6488.RA0WHQGMDQ3IhTUlElkPioAJodNUil6EFeRrngoPFhL2g130_provenance.