Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP149952.RA9yN8FmTk6xUCv8_P3M1wG1y-lqM9I9tZcFOVjNbeRlw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP149952.RA9yN8FmTk6xUCv8_P3M1wG1y-lqM9I9tZcFOVjNbeRlw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP149952.RA9yN8FmTk6xUCv8_P3M1wG1y-lqM9I9tZcFOVjNbeRlw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP149952.RA9yN8FmTk6xUCv8_P3M1wG1y-lqM9I9tZcFOVjNbeRlw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP149952.RA9yN8FmTk6xUCv8_P3M1wG1y-lqM9I9tZcFOVjNbeRlw130_provenance.
- NP149952.RA9yN8FmTk6xUCv8_P3M1wG1y-lqM9I9tZcFOVjNbeRlw130_assertion wasGeneratedBy ECO_0000203 NP149952.RA9yN8FmTk6xUCv8_P3M1wG1y-lqM9I9tZcFOVjNbeRlw130_provenance.
- NP149952.RA9yN8FmTk6xUCv8_P3M1wG1y-lqM9I9tZcFOVjNbeRlw130_assertion wasDerivedFrom gad-20150221 NP149952.RA9yN8FmTk6xUCv8_P3M1wG1y-lqM9I9tZcFOVjNbeRlw130_provenance.
- NP149952.RA9yN8FmTk6xUCv8_P3M1wG1y-lqM9I9tZcFOVjNbeRlw130_assertion SIO_000772 20663923 NP149952.RA9yN8FmTk6xUCv8_P3M1wG1y-lqM9I9tZcFOVjNbeRlw130_provenance.
- NP149952.RA9yN8FmTk6xUCv8_P3M1wG1y-lqM9I9tZcFOVjNbeRlw130_assertion evidence source_evidence_literature NP149952.RA9yN8FmTk6xUCv8_P3M1wG1y-lqM9I9tZcFOVjNbeRlw130_provenance.
- NP149952.RA9yN8FmTk6xUCv8_P3M1wG1y-lqM9I9tZcFOVjNbeRlw130_assertion description "[A genome-wide scan for common alleles affecting risk for autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149952.RA9yN8FmTk6xUCv8_P3M1wG1y-lqM9I9tZcFOVjNbeRlw130_provenance.