Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959085.RA6YQDhKhHAjqD33UVKnXcNaS7kaHm-CzOafIYYvhnfnI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP959085.RA6YQDhKhHAjqD33UVKnXcNaS7kaHm-CzOafIYYvhnfnI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959085.RA6YQDhKhHAjqD33UVKnXcNaS7kaHm-CzOafIYYvhnfnI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959085.RA6YQDhKhHAjqD33UVKnXcNaS7kaHm-CzOafIYYvhnfnI130_provenance.
- NP959085.RA6YQDhKhHAjqD33UVKnXcNaS7kaHm-CzOafIYYvhnfnI130_assertion description "[A large number of these corresponded to genomic regions or genes (ATP13A4, CDH9, CDH13, CNTNAP2, CTNNA3, DIAPH3, GRIN2A, MDGA2, SHANK3) that have been either associated with ASD for most of them, or involved in speech or language impairment, or in RE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959085.RA6YQDhKhHAjqD33UVKnXcNaS7kaHm-CzOafIYYvhnfnI130_provenance.
- NP959085.RA6YQDhKhHAjqD33UVKnXcNaS7kaHm-CzOafIYYvhnfnI130_assertion evidence source_evidence_literature NP959085.RA6YQDhKhHAjqD33UVKnXcNaS7kaHm-CzOafIYYvhnfnI130_provenance.
- NP959085.RA6YQDhKhHAjqD33UVKnXcNaS7kaHm-CzOafIYYvhnfnI130_assertion SIO_000772 22738016 NP959085.RA6YQDhKhHAjqD33UVKnXcNaS7kaHm-CzOafIYYvhnfnI130_provenance.
- NP959085.RA6YQDhKhHAjqD33UVKnXcNaS7kaHm-CzOafIYYvhnfnI130_assertion wasDerivedFrom befree-20150227 NP959085.RA6YQDhKhHAjqD33UVKnXcNaS7kaHm-CzOafIYYvhnfnI130_provenance.
- NP959085.RA6YQDhKhHAjqD33UVKnXcNaS7kaHm-CzOafIYYvhnfnI130_assertion wasGeneratedBy ECO_0000203 NP959085.RA6YQDhKhHAjqD33UVKnXcNaS7kaHm-CzOafIYYvhnfnI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP959085.RA6YQDhKhHAjqD33UVKnXcNaS7kaHm-CzOafIYYvhnfnI130_provenance.