Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP523464.RABwAJ6oog0r48jjBnzUg1e8yKtcvP1woi9ceU1MxmfGw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP523464.RABwAJ6oog0r48jjBnzUg1e8yKtcvP1woi9ceU1MxmfGw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523464.RABwAJ6oog0r48jjBnzUg1e8yKtcvP1woi9ceU1MxmfGw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523464.RABwAJ6oog0r48jjBnzUg1e8yKtcvP1woi9ceU1MxmfGw130_provenance.
- NP523464.RABwAJ6oog0r48jjBnzUg1e8yKtcvP1woi9ceU1MxmfGw130_assertion wasGeneratedBy ECO_0000203 NP523464.RABwAJ6oog0r48jjBnzUg1e8yKtcvP1woi9ceU1MxmfGw130_provenance.
- NP523464.RABwAJ6oog0r48jjBnzUg1e8yKtcvP1woi9ceU1MxmfGw130_assertion wasDerivedFrom befree-20140225 NP523464.RABwAJ6oog0r48jjBnzUg1e8yKtcvP1woi9ceU1MxmfGw130_provenance.
- NP523464.RABwAJ6oog0r48jjBnzUg1e8yKtcvP1woi9ceU1MxmfGw130_assertion SIO_000772 7888141 NP523464.RABwAJ6oog0r48jjBnzUg1e8yKtcvP1woi9ceU1MxmfGw130_provenance.
- NP523464.RABwAJ6oog0r48jjBnzUg1e8yKtcvP1woi9ceU1MxmfGw130_assertion evidence source_evidence_literature NP523464.RABwAJ6oog0r48jjBnzUg1e8yKtcvP1woi9ceU1MxmfGw130_provenance.
- NP523464.RABwAJ6oog0r48jjBnzUg1e8yKtcvP1woi9ceU1MxmfGw130_assertion description "[The findings in the present family illustrate that the typical characteristics of the fragile X syndrome can be caused by other types of mutations involving the FMR1 than the highly expanded stretches of CGG repeats in the 5' noncoding region of the FMR1 gene, coinciding with abnormal methylation patterns in that area as present in the vast majority of individuals with the fragile X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523464.RABwAJ6oog0r48jjBnzUg1e8yKtcvP1woi9ceU1MxmfGw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP523464.RABwAJ6oog0r48jjBnzUg1e8yKtcvP1woi9ceU1MxmfGw130_provenance.