Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP293332.RAzK2S7kCh2phyPQbd2ELNVQE8unmgRBr3iVfJW97qvW4130_provenance.