Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP831091.RAa-DxtyW94ARa2iW4bRlxpPd3xvjNhOt7y85PeMaMZAk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP831091.RAa-DxtyW94ARa2iW4bRlxpPd3xvjNhOt7y85PeMaMZAk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831091.RAa-DxtyW94ARa2iW4bRlxpPd3xvjNhOt7y85PeMaMZAk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831091.RAa-DxtyW94ARa2iW4bRlxpPd3xvjNhOt7y85PeMaMZAk130_provenance.
- NP831091.RAa-DxtyW94ARa2iW4bRlxpPd3xvjNhOt7y85PeMaMZAk130_assertion wasGeneratedBy ECO_0000203 NP831091.RAa-DxtyW94ARa2iW4bRlxpPd3xvjNhOt7y85PeMaMZAk130_provenance.
- NP831091.RAa-DxtyW94ARa2iW4bRlxpPd3xvjNhOt7y85PeMaMZAk130_assertion wasDerivedFrom befree-20140225 NP831091.RAa-DxtyW94ARa2iW4bRlxpPd3xvjNhOt7y85PeMaMZAk130_provenance.
- NP831091.RAa-DxtyW94ARa2iW4bRlxpPd3xvjNhOt7y85PeMaMZAk130_assertion SIO_000772 11311134 NP831091.RAa-DxtyW94ARa2iW4bRlxpPd3xvjNhOt7y85PeMaMZAk130_provenance.
- NP831091.RAa-DxtyW94ARa2iW4bRlxpPd3xvjNhOt7y85PeMaMZAk130_assertion evidence source_evidence_literature NP831091.RAa-DxtyW94ARa2iW4bRlxpPd3xvjNhOt7y85PeMaMZAk130_provenance.
- NP831091.RAa-DxtyW94ARa2iW4bRlxpPd3xvjNhOt7y85PeMaMZAk130_assertion description "[These results suggest that BM88 may be a candidate gene for genetic disorders associated with alterations at 11p15.5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831091.RAa-DxtyW94ARa2iW4bRlxpPd3xvjNhOt7y85PeMaMZAk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP831091.RAa-DxtyW94ARa2iW4bRlxpPd3xvjNhOt7y85PeMaMZAk130_provenance.