Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP380522.RAHDtG3aIIvEqxP85zlLM5RNkaBdw7xmxM18f37NH2zac130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP380522.RAHDtG3aIIvEqxP85zlLM5RNkaBdw7xmxM18f37NH2zac130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP380522.RAHDtG3aIIvEqxP85zlLM5RNkaBdw7xmxM18f37NH2zac130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP380522.RAHDtG3aIIvEqxP85zlLM5RNkaBdw7xmxM18f37NH2zac130_provenance.
- NP380522.RAHDtG3aIIvEqxP85zlLM5RNkaBdw7xmxM18f37NH2zac130_assertion description "[Together, these results support a model where the DIA1 and DIA1R gene products regulate molecular traffic through the cellular secretory pathway or affect the function of secreted factors, and functional deficits cause disorders with ASD-like symptoms and/or mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380522.RAHDtG3aIIvEqxP85zlLM5RNkaBdw7xmxM18f37NH2zac130_provenance.
- NP380522.RAHDtG3aIIvEqxP85zlLM5RNkaBdw7xmxM18f37NH2zac130_assertion evidence source_evidence_literature NP380522.RAHDtG3aIIvEqxP85zlLM5RNkaBdw7xmxM18f37NH2zac130_provenance.
- NP380522.RAHDtG3aIIvEqxP85zlLM5RNkaBdw7xmxM18f37NH2zac130_assertion SIO_000772 21264219 NP380522.RAHDtG3aIIvEqxP85zlLM5RNkaBdw7xmxM18f37NH2zac130_provenance.
- NP380522.RAHDtG3aIIvEqxP85zlLM5RNkaBdw7xmxM18f37NH2zac130_assertion wasDerivedFrom befree-20140225 NP380522.RAHDtG3aIIvEqxP85zlLM5RNkaBdw7xmxM18f37NH2zac130_provenance.
- NP380522.RAHDtG3aIIvEqxP85zlLM5RNkaBdw7xmxM18f37NH2zac130_assertion wasGeneratedBy ECO_0000203 NP380522.RAHDtG3aIIvEqxP85zlLM5RNkaBdw7xmxM18f37NH2zac130_provenance.
- befree-20140225 importedOn "2014-02-25" NP380522.RAHDtG3aIIvEqxP85zlLM5RNkaBdw7xmxM18f37NH2zac130_provenance.