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- source_evidence_literature type ECO_0000212 NP428387.RAa7lO_Ywn1o-p9nLicYUTHGD71EFNfaLfhDnLi24W5ZU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428387.RAa7lO_Ywn1o-p9nLicYUTHGD71EFNfaLfhDnLi24W5ZU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428387.RAa7lO_Ywn1o-p9nLicYUTHGD71EFNfaLfhDnLi24W5ZU130_provenance.
- NP428387.RAa7lO_Ywn1o-p9nLicYUTHGD71EFNfaLfhDnLi24W5ZU130_assertion description "[Fragile X syndrome, the most common heritable form of cognitive impairment, is caused by epigenetic silencing of the fragile X (FMR1) gene owing to large expansions (>200 repeats) of a non-coding CGG-repeat element.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428387.RAa7lO_Ywn1o-p9nLicYUTHGD71EFNfaLfhDnLi24W5ZU130_provenance.
- NP428387.RAa7lO_Ywn1o-p9nLicYUTHGD71EFNfaLfhDnLi24W5ZU130_assertion evidence source_evidence_literature NP428387.RAa7lO_Ywn1o-p9nLicYUTHGD71EFNfaLfhDnLi24W5ZU130_provenance.
- NP428387.RAa7lO_Ywn1o-p9nLicYUTHGD71EFNfaLfhDnLi24W5ZU130_assertion SIO_000772 23867198 NP428387.RAa7lO_Ywn1o-p9nLicYUTHGD71EFNfaLfhDnLi24W5ZU130_provenance.
- NP428387.RAa7lO_Ywn1o-p9nLicYUTHGD71EFNfaLfhDnLi24W5ZU130_assertion wasDerivedFrom befree-20140225 NP428387.RAa7lO_Ywn1o-p9nLicYUTHGD71EFNfaLfhDnLi24W5ZU130_provenance.
- NP428387.RAa7lO_Ywn1o-p9nLicYUTHGD71EFNfaLfhDnLi24W5ZU130_assertion wasGeneratedBy ECO_0000203 NP428387.RAa7lO_Ywn1o-p9nLicYUTHGD71EFNfaLfhDnLi24W5ZU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP428387.RAa7lO_Ywn1o-p9nLicYUTHGD71EFNfaLfhDnLi24W5ZU130_provenance.