Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP960743.RAR3eKWpA2z1IMmN91PPnZcdLNAz2WFiraYzKHsJh95X8130_assertion> ?p ?o ?g. }
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- NP960743.RAR3eKWpA2z1IMmN91PPnZcdLNAz2WFiraYzKHsJh95X8130_assertion type Assertion NP960743.RAR3eKWpA2z1IMmN91PPnZcdLNAz2WFiraYzKHsJh95X8130_head.
- NP960743.RAR3eKWpA2z1IMmN91PPnZcdLNAz2WFiraYzKHsJh95X8130_assertion description "[In our previous study, we have identified a homozygous TMEM67 mutation in a Chinese family exhibiting clinical characteristics of MKS3, which provided a ground for further PGD procedure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960743.RAR3eKWpA2z1IMmN91PPnZcdLNAz2WFiraYzKHsJh95X8130_provenance.
- NP960743.RAR3eKWpA2z1IMmN91PPnZcdLNAz2WFiraYzKHsJh95X8130_assertion evidence source_evidence_literature NP960743.RAR3eKWpA2z1IMmN91PPnZcdLNAz2WFiraYzKHsJh95X8130_provenance.
- NP960743.RAR3eKWpA2z1IMmN91PPnZcdLNAz2WFiraYzKHsJh95X8130_assertion SIO_000772 24039893 NP960743.RAR3eKWpA2z1IMmN91PPnZcdLNAz2WFiraYzKHsJh95X8130_provenance.
- NP960743.RAR3eKWpA2z1IMmN91PPnZcdLNAz2WFiraYzKHsJh95X8130_assertion wasDerivedFrom befree-20150227 NP960743.RAR3eKWpA2z1IMmN91PPnZcdLNAz2WFiraYzKHsJh95X8130_provenance.
- NP960743.RAR3eKWpA2z1IMmN91PPnZcdLNAz2WFiraYzKHsJh95X8130_assertion wasGeneratedBy ECO_0000203 NP960743.RAR3eKWpA2z1IMmN91PPnZcdLNAz2WFiraYzKHsJh95X8130_provenance.