Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_assertion> ?p ?o ?g. }
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- NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_assertion type Assertion NP253473.RAeIsZHZ2XV-J5jbpLtNSA_UFSN76M98V009VjPzkk2LQ130_head.
- 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.