Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP408675.RANOJV8nFR-sbl6snNId5Ld1mOvRImq1GsL270iwx_i50130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP408675.RANOJV8nFR-sbl6snNId5Ld1mOvRImq1GsL270iwx_i50130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP408675.RANOJV8nFR-sbl6snNId5Ld1mOvRImq1GsL270iwx_i50130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP408675.RANOJV8nFR-sbl6snNId5Ld1mOvRImq1GsL270iwx_i50130_provenance.
- NP408675.RANOJV8nFR-sbl6snNId5Ld1mOvRImq1GsL270iwx_i50130_assertion description "[However, the recent documentation of abnormal elevation of FMR1 mRNA, discovery of fragile X-associated tremor/ataxia syndrome (FXTAS), and reports of psychiatric disorders in children and adults with the premutation have suggested a pathogenic gene-brain-behavior mechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408675.RANOJV8nFR-sbl6snNId5Ld1mOvRImq1GsL270iwx_i50130_provenance.
- NP408675.RANOJV8nFR-sbl6snNId5Ld1mOvRImq1GsL270iwx_i50130_assertion evidence source_evidence_literature NP408675.RANOJV8nFR-sbl6snNId5Ld1mOvRImq1GsL270iwx_i50130_provenance.
- NP408675.RANOJV8nFR-sbl6snNId5Ld1mOvRImq1GsL270iwx_i50130_assertion SIO_000772 16184602 NP408675.RANOJV8nFR-sbl6snNId5Ld1mOvRImq1GsL270iwx_i50130_provenance.
- NP408675.RANOJV8nFR-sbl6snNId5Ld1mOvRImq1GsL270iwx_i50130_assertion wasDerivedFrom befree-20150227 NP408675.RANOJV8nFR-sbl6snNId5Ld1mOvRImq1GsL270iwx_i50130_provenance.
- NP408675.RANOJV8nFR-sbl6snNId5Ld1mOvRImq1GsL270iwx_i50130_assertion wasGeneratedBy ECO_0000203 NP408675.RANOJV8nFR-sbl6snNId5Ld1mOvRImq1GsL270iwx_i50130_provenance.
- befree-20150227 importedOn "2015-02-27" NP408675.RANOJV8nFR-sbl6snNId5Ld1mOvRImq1GsL270iwx_i50130_provenance.