Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_provenance.
- NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_assertion wasGeneratedBy ECO_0000203 NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_provenance.
- NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_assertion wasDerivedFrom befree-2016 NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_provenance.
- NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_assertion SIO_000772 10341296 NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_provenance.
- NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_assertion evidence source_evidence_literature NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_provenance.
- NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_assertion description "[The fragile X syndrome is due to the shutdown of the FMR1 gene transcription, and the pathogenesis of this syndrome is a consequence of absence of the protein product of the FMR1 gene (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_provenance.