Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3716.RAd8SvbtMPCp9T981gOmUUBkaz7LgihF2-2t10WNrokMU130_assertion> ?p ?o ?g. }
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- NP3716.RAd8SvbtMPCp9T981gOmUUBkaz7LgihF2-2t10WNrokMU130_assertion type Assertion NP3716.RAd8SvbtMPCp9T981gOmUUBkaz7LgihF2-2t10WNrokMU130_head.
- NP3716.RAd8SvbtMPCp9T981gOmUUBkaz7LgihF2-2t10WNrokMU130_assertion wasGeneratedBy ECO_0000218 NP3716.RAd8SvbtMPCp9T981gOmUUBkaz7LgihF2-2t10WNrokMU130_provenance.
- NP3716.RAd8SvbtMPCp9T981gOmUUBkaz7LgihF2-2t10WNrokMU130_assertion wasDerivedFrom uniprot-20130724 NP3716.RAd8SvbtMPCp9T981gOmUUBkaz7LgihF2-2t10WNrokMU130_provenance.
- NP3716.RAd8SvbtMPCp9T981gOmUUBkaz7LgihF2-2t10WNrokMU130_assertion SIO_000772 21236492 NP3716.RAd8SvbtMPCp9T981gOmUUBkaz7LgihF2-2t10WNrokMU130_provenance.
- NP3716.RAd8SvbtMPCp9T981gOmUUBkaz7LgihF2-2t10WNrokMU130_assertion evidence source_evidence_curated NP3716.RAd8SvbtMPCp9T981gOmUUBkaz7LgihF2-2t10WNrokMU130_provenance.
- NP3716.RAd8SvbtMPCp9T981gOmUUBkaz7LgihF2-2t10WNrokMU130_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." NP3716.RAd8SvbtMPCp9T981gOmUUBkaz7LgihF2-2t10WNrokMU130_provenance.