Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP321881.RAr1PD9tBwm-wB4-7IzsqJPv6NziFMfuJVaiV4cHadENw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP321881.RAr1PD9tBwm-wB4-7IzsqJPv6NziFMfuJVaiV4cHadENw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP321881.RAr1PD9tBwm-wB4-7IzsqJPv6NziFMfuJVaiV4cHadENw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP321881.RAr1PD9tBwm-wB4-7IzsqJPv6NziFMfuJVaiV4cHadENw130_provenance.
- NP321881.RAr1PD9tBwm-wB4-7IzsqJPv6NziFMfuJVaiV4cHadENw130_assertion description "[Smaller, so-called premutation expansions (55-200 repeats) can cause a family of neurodevelopmental phenotypes (attention deficit hyperactivity disorder, autism spectrum disorder, seizure disorder) and neurodegenerative (fragile X-associated tremor/ataxia syndrome [FXTAS]) phenotypes through an entirely distinct molecular mechanism involving increased FMR1 mRNA production and toxicity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321881.RAr1PD9tBwm-wB4-7IzsqJPv6NziFMfuJVaiV4cHadENw130_provenance.
- NP321881.RAr1PD9tBwm-wB4-7IzsqJPv6NziFMfuJVaiV4cHadENw130_assertion evidence source_evidence_literature NP321881.RAr1PD9tBwm-wB4-7IzsqJPv6NziFMfuJVaiV4cHadENw130_provenance.
- NP321881.RAr1PD9tBwm-wB4-7IzsqJPv6NziFMfuJVaiV4cHadENw130_assertion SIO_000772 23867198 NP321881.RAr1PD9tBwm-wB4-7IzsqJPv6NziFMfuJVaiV4cHadENw130_provenance.
- NP321881.RAr1PD9tBwm-wB4-7IzsqJPv6NziFMfuJVaiV4cHadENw130_assertion wasDerivedFrom befree-20140225 NP321881.RAr1PD9tBwm-wB4-7IzsqJPv6NziFMfuJVaiV4cHadENw130_provenance.
- NP321881.RAr1PD9tBwm-wB4-7IzsqJPv6NziFMfuJVaiV4cHadENw130_assertion wasGeneratedBy ECO_0000203 NP321881.RAr1PD9tBwm-wB4-7IzsqJPv6NziFMfuJVaiV4cHadENw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP321881.RAr1PD9tBwm-wB4-7IzsqJPv6NziFMfuJVaiV4cHadENw130_provenance.