Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_assertion> ?p ?o ?g. }
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- NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_assertion type Assertion NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_head.
- NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_assertion description "[Here, we report the finding that MCPH1 primary microcephaly and PCC syndrome are allelic disorders, both having mutations in the MCPH1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_provenance.
- NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_assertion evidence source_evidence_literature NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_provenance.
- NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_assertion SIO_000772 15199523 NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_provenance.
- NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_assertion wasDerivedFrom befree-20140225 NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_provenance.
- NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_assertion wasGeneratedBy ECO_0000203 NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_provenance.