Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP593381.RAuFaxNz_QZqU6P7IqZrgZS3x9E6sHZ18wR_yvzYDsZm0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP593381.RAuFaxNz_QZqU6P7IqZrgZS3x9E6sHZ18wR_yvzYDsZm0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP593381.RAuFaxNz_QZqU6P7IqZrgZS3x9E6sHZ18wR_yvzYDsZm0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP593381.RAuFaxNz_QZqU6P7IqZrgZS3x9E6sHZ18wR_yvzYDsZm0130_provenance.
- NP593381.RAuFaxNz_QZqU6P7IqZrgZS3x9E6sHZ18wR_yvzYDsZm0130_assertion description "[Fragile X syndrome is primarily due to a CGG repeat expansion found in the FMR1 X-linked gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593381.RAuFaxNz_QZqU6P7IqZrgZS3x9E6sHZ18wR_yvzYDsZm0130_provenance.
- NP593381.RAuFaxNz_QZqU6P7IqZrgZS3x9E6sHZ18wR_yvzYDsZm0130_assertion evidence source_evidence_literature NP593381.RAuFaxNz_QZqU6P7IqZrgZS3x9E6sHZ18wR_yvzYDsZm0130_provenance.
- NP593381.RAuFaxNz_QZqU6P7IqZrgZS3x9E6sHZ18wR_yvzYDsZm0130_assertion SIO_000772 17295053 NP593381.RAuFaxNz_QZqU6P7IqZrgZS3x9E6sHZ18wR_yvzYDsZm0130_provenance.
- NP593381.RAuFaxNz_QZqU6P7IqZrgZS3x9E6sHZ18wR_yvzYDsZm0130_assertion wasDerivedFrom befree-2016 NP593381.RAuFaxNz_QZqU6P7IqZrgZS3x9E6sHZ18wR_yvzYDsZm0130_provenance.
- NP593381.RAuFaxNz_QZqU6P7IqZrgZS3x9E6sHZ18wR_yvzYDsZm0130_assertion wasGeneratedBy ECO_0000203 NP593381.RAuFaxNz_QZqU6P7IqZrgZS3x9E6sHZ18wR_yvzYDsZm0130_provenance.
- befree-2016 importedOn "2016-02-19" NP593381.RAuFaxNz_QZqU6P7IqZrgZS3x9E6sHZ18wR_yvzYDsZm0130_provenance.