Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP405998.RA1I2PDd5jvhJDgDFwp37P67aZXWc1Yq6hGyjC7GutRkY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP405998.RA1I2PDd5jvhJDgDFwp37P67aZXWc1Yq6hGyjC7GutRkY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP405998.RA1I2PDd5jvhJDgDFwp37P67aZXWc1Yq6hGyjC7GutRkY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP405998.RA1I2PDd5jvhJDgDFwp37P67aZXWc1Yq6hGyjC7GutRkY130_provenance.
- NP405998.RA1I2PDd5jvhJDgDFwp37P67aZXWc1Yq6hGyjC7GutRkY130_assertion wasGeneratedBy ECO_0000203 NP405998.RA1I2PDd5jvhJDgDFwp37P67aZXWc1Yq6hGyjC7GutRkY130_provenance.
- NP405998.RA1I2PDd5jvhJDgDFwp37P67aZXWc1Yq6hGyjC7GutRkY130_assertion wasDerivedFrom befree-20140225 NP405998.RA1I2PDd5jvhJDgDFwp37P67aZXWc1Yq6hGyjC7GutRkY130_provenance.
- NP405998.RA1I2PDd5jvhJDgDFwp37P67aZXWc1Yq6hGyjC7GutRkY130_assertion SIO_000772 21035104 NP405998.RA1I2PDd5jvhJDgDFwp37P67aZXWc1Yq6hGyjC7GutRkY130_provenance.
- NP405998.RA1I2PDd5jvhJDgDFwp37P67aZXWc1Yq6hGyjC7GutRkY130_assertion evidence source_evidence_literature NP405998.RA1I2PDd5jvhJDgDFwp37P67aZXWc1Yq6hGyjC7GutRkY130_provenance.
- NP405998.RA1I2PDd5jvhJDgDFwp37P67aZXWc1Yq6hGyjC7GutRkY130_assertion description "[We have identified missense mutations in prodynorphin (PDYN) that cause SCA23 in four Dutch families displaying progressive gait and limb ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP405998.RA1I2PDd5jvhJDgDFwp37P67aZXWc1Yq6hGyjC7GutRkY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP405998.RA1I2PDd5jvhJDgDFwp37P67aZXWc1Yq6hGyjC7GutRkY130_provenance.