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- source_evidence_literature type ECO_0000212 NP645117.RAyi2PTjWhqn7olYFsgWzHqg2tz3fc9kGFdTpXORpu_G8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP645117.RAyi2PTjWhqn7olYFsgWzHqg2tz3fc9kGFdTpXORpu_G8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP645117.RAyi2PTjWhqn7olYFsgWzHqg2tz3fc9kGFdTpXORpu_G8130_provenance.
- NP645117.RAyi2PTjWhqn7olYFsgWzHqg2tz3fc9kGFdTpXORpu_G8130_assertion description "[Mental retardation in this syndrome is considered as resulting from the abolition of the FMR1 gene expression due to hypermethylation of the gene CpG islands adjacent to the expanded methylated trinucleotide repeat.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645117.RAyi2PTjWhqn7olYFsgWzHqg2tz3fc9kGFdTpXORpu_G8130_provenance.
- NP645117.RAyi2PTjWhqn7olYFsgWzHqg2tz3fc9kGFdTpXORpu_G8130_assertion evidence source_evidence_literature NP645117.RAyi2PTjWhqn7olYFsgWzHqg2tz3fc9kGFdTpXORpu_G8130_provenance.
- NP645117.RAyi2PTjWhqn7olYFsgWzHqg2tz3fc9kGFdTpXORpu_G8130_assertion SIO_000772 18078840 NP645117.RAyi2PTjWhqn7olYFsgWzHqg2tz3fc9kGFdTpXORpu_G8130_provenance.
- NP645117.RAyi2PTjWhqn7olYFsgWzHqg2tz3fc9kGFdTpXORpu_G8130_assertion wasDerivedFrom befree-2016 NP645117.RAyi2PTjWhqn7olYFsgWzHqg2tz3fc9kGFdTpXORpu_G8130_provenance.
- NP645117.RAyi2PTjWhqn7olYFsgWzHqg2tz3fc9kGFdTpXORpu_G8130_assertion wasGeneratedBy ECO_0000203 NP645117.RAyi2PTjWhqn7olYFsgWzHqg2tz3fc9kGFdTpXORpu_G8130_provenance.
- befree-2016 importedOn "2016-02-19" NP645117.RAyi2PTjWhqn7olYFsgWzHqg2tz3fc9kGFdTpXORpu_G8130_provenance.