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- source_evidence_literature type ECO_0000212 NP978350.RA9my_WjHPxBBVCKokBXvZQRVMgtSUwyuiJYJpDfVmeng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978350.RA9my_WjHPxBBVCKokBXvZQRVMgtSUwyuiJYJpDfVmeng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978350.RA9my_WjHPxBBVCKokBXvZQRVMgtSUwyuiJYJpDfVmeng130_provenance.
- NP978350.RA9my_WjHPxBBVCKokBXvZQRVMgtSUwyuiJYJpDfVmeng130_assertion description "[Our data suggest that ADAMTS18 plays an essential role in early eye development and that mutations therein cause a distinct eye phenotype that is mainly characterized by microcornea and myopia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978350.RA9my_WjHPxBBVCKokBXvZQRVMgtSUwyuiJYJpDfVmeng130_provenance.
- NP978350.RA9my_WjHPxBBVCKokBXvZQRVMgtSUwyuiJYJpDfVmeng130_assertion evidence source_evidence_literature NP978350.RA9my_WjHPxBBVCKokBXvZQRVMgtSUwyuiJYJpDfVmeng130_provenance.
- NP978350.RA9my_WjHPxBBVCKokBXvZQRVMgtSUwyuiJYJpDfVmeng130_assertion SIO_000772 23818446 NP978350.RA9my_WjHPxBBVCKokBXvZQRVMgtSUwyuiJYJpDfVmeng130_provenance.
- NP978350.RA9my_WjHPxBBVCKokBXvZQRVMgtSUwyuiJYJpDfVmeng130_assertion wasDerivedFrom befree-20150227 NP978350.RA9my_WjHPxBBVCKokBXvZQRVMgtSUwyuiJYJpDfVmeng130_provenance.
- NP978350.RA9my_WjHPxBBVCKokBXvZQRVMgtSUwyuiJYJpDfVmeng130_assertion wasGeneratedBy ECO_0000203 NP978350.RA9my_WjHPxBBVCKokBXvZQRVMgtSUwyuiJYJpDfVmeng130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978350.RA9my_WjHPxBBVCKokBXvZQRVMgtSUwyuiJYJpDfVmeng130_provenance.