Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978620.RAQgcO2hwln-l5lk8eMW9LGPqDwPmUrUpoUzCclrw6gxk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978620.RAQgcO2hwln-l5lk8eMW9LGPqDwPmUrUpoUzCclrw6gxk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978620.RAQgcO2hwln-l5lk8eMW9LGPqDwPmUrUpoUzCclrw6gxk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978620.RAQgcO2hwln-l5lk8eMW9LGPqDwPmUrUpoUzCclrw6gxk130_provenance.
- NP978620.RAQgcO2hwln-l5lk8eMW9LGPqDwPmUrUpoUzCclrw6gxk130_assertion description "[We used a series of polymorphic markers mapped to chromosome 7 to test this hypothesis in 22 children with MPS and MDS, including 19 with JCML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978620.RAQgcO2hwln-l5lk8eMW9LGPqDwPmUrUpoUzCclrw6gxk130_provenance.
- NP978620.RAQgcO2hwln-l5lk8eMW9LGPqDwPmUrUpoUzCclrw6gxk130_assertion evidence source_evidence_literature NP978620.RAQgcO2hwln-l5lk8eMW9LGPqDwPmUrUpoUzCclrw6gxk130_provenance.
- NP978620.RAQgcO2hwln-l5lk8eMW9LGPqDwPmUrUpoUzCclrw6gxk130_assertion SIO_000772 7534111 NP978620.RAQgcO2hwln-l5lk8eMW9LGPqDwPmUrUpoUzCclrw6gxk130_provenance.
- NP978620.RAQgcO2hwln-l5lk8eMW9LGPqDwPmUrUpoUzCclrw6gxk130_assertion wasDerivedFrom befree-20150227 NP978620.RAQgcO2hwln-l5lk8eMW9LGPqDwPmUrUpoUzCclrw6gxk130_provenance.
- NP978620.RAQgcO2hwln-l5lk8eMW9LGPqDwPmUrUpoUzCclrw6gxk130_assertion wasGeneratedBy ECO_0000203 NP978620.RAQgcO2hwln-l5lk8eMW9LGPqDwPmUrUpoUzCclrw6gxk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978620.RAQgcO2hwln-l5lk8eMW9LGPqDwPmUrUpoUzCclrw6gxk130_provenance.