Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP786837.RAsv4iAoxvfSjJJ_velzj4V5sfflvzKrbyFR7oLUmKy8U130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP786837.RAsv4iAoxvfSjJJ_velzj4V5sfflvzKrbyFR7oLUmKy8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP786837.RAsv4iAoxvfSjJJ_velzj4V5sfflvzKrbyFR7oLUmKy8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP786837.RAsv4iAoxvfSjJJ_velzj4V5sfflvzKrbyFR7oLUmKy8U130_provenance.
- NP786837.RAsv4iAoxvfSjJJ_velzj4V5sfflvzKrbyFR7oLUmKy8U130_assertion description "[Here, we describe the positional cloning of SCAMP5, CLIC4 and PPCDC as candidate genes for autism, starting from a person with idiopathic, sporadic autism carrying a de novo chromosomal translocation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP786837.RAsv4iAoxvfSjJJ_velzj4V5sfflvzKrbyFR7oLUmKy8U130_provenance.
- NP786837.RAsv4iAoxvfSjJJ_velzj4V5sfflvzKrbyFR7oLUmKy8U130_assertion evidence source_evidence_literature NP786837.RAsv4iAoxvfSjJJ_velzj4V5sfflvzKrbyFR7oLUmKy8U130_provenance.
- NP786837.RAsv4iAoxvfSjJJ_velzj4V5sfflvzKrbyFR7oLUmKy8U130_assertion SIO_000772 20071347 NP786837.RAsv4iAoxvfSjJJ_velzj4V5sfflvzKrbyFR7oLUmKy8U130_provenance.
- NP786837.RAsv4iAoxvfSjJJ_velzj4V5sfflvzKrbyFR7oLUmKy8U130_assertion wasDerivedFrom befree-2016 NP786837.RAsv4iAoxvfSjJJ_velzj4V5sfflvzKrbyFR7oLUmKy8U130_provenance.
- NP786837.RAsv4iAoxvfSjJJ_velzj4V5sfflvzKrbyFR7oLUmKy8U130_assertion wasGeneratedBy ECO_0000203 NP786837.RAsv4iAoxvfSjJJ_velzj4V5sfflvzKrbyFR7oLUmKy8U130_provenance.
- befree-2016 importedOn "2016-02-19" NP786837.RAsv4iAoxvfSjJJ_velzj4V5sfflvzKrbyFR7oLUmKy8U130_provenance.