Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP836309.RAlYL-_i4Yti2eiUr_z4Wg98T4Y1uKfoFfqBAgVVHZJbE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP836309.RAlYL-_i4Yti2eiUr_z4Wg98T4Y1uKfoFfqBAgVVHZJbE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP836309.RAlYL-_i4Yti2eiUr_z4Wg98T4Y1uKfoFfqBAgVVHZJbE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP836309.RAlYL-_i4Yti2eiUr_z4Wg98T4Y1uKfoFfqBAgVVHZJbE130_provenance.
- NP836309.RAlYL-_i4Yti2eiUr_z4Wg98T4Y1uKfoFfqBAgVVHZJbE130_assertion description "[For four mutations affecting ATRX (p.1761M>T), PQBP1 (p.155R>X) and SLC6A8 (p.390P>L and p.477S>L), we provide evidence for a functional involvement of these changes in the aetiology of intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836309.RAlYL-_i4Yti2eiUr_z4Wg98T4Y1uKfoFfqBAgVVHZJbE130_provenance.
- NP836309.RAlYL-_i4Yti2eiUr_z4Wg98T4Y1uKfoFfqBAgVVHZJbE130_assertion evidence source_evidence_literature NP836309.RAlYL-_i4Yti2eiUr_z4Wg98T4Y1uKfoFfqBAgVVHZJbE130_provenance.
- NP836309.RAlYL-_i4Yti2eiUr_z4Wg98T4Y1uKfoFfqBAgVVHZJbE130_assertion SIO_000772 21267006 NP836309.RAlYL-_i4Yti2eiUr_z4Wg98T4Y1uKfoFfqBAgVVHZJbE130_provenance.
- NP836309.RAlYL-_i4Yti2eiUr_z4Wg98T4Y1uKfoFfqBAgVVHZJbE130_assertion wasDerivedFrom befree-20150227 NP836309.RAlYL-_i4Yti2eiUr_z4Wg98T4Y1uKfoFfqBAgVVHZJbE130_provenance.
- NP836309.RAlYL-_i4Yti2eiUr_z4Wg98T4Y1uKfoFfqBAgVVHZJbE130_assertion wasGeneratedBy ECO_0000203 NP836309.RAlYL-_i4Yti2eiUr_z4Wg98T4Y1uKfoFfqBAgVVHZJbE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP836309.RAlYL-_i4Yti2eiUr_z4Wg98T4Y1uKfoFfqBAgVVHZJbE130_provenance.