Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP881352.RA2Tx9cYLvwPhoH43Q3tXVL-hPymCLxhDk4mrfYgs2JfQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881352.RA2Tx9cYLvwPhoH43Q3tXVL-hPymCLxhDk4mrfYgs2JfQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881352.RA2Tx9cYLvwPhoH43Q3tXVL-hPymCLxhDk4mrfYgs2JfQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881352.RA2Tx9cYLvwPhoH43Q3tXVL-hPymCLxhDk4mrfYgs2JfQ130_provenance.
- NP881352.RA2Tx9cYLvwPhoH43Q3tXVL-hPymCLxhDk4mrfYgs2JfQ130_assertion description "[Although genetic variations in several genes encoding for synaptic adhesion proteins have been found to be associated with autism spectrum disorders, one of the most consistently replicated genes has been CNTNAP2, encoding for contactin-associated protein-like 2 (CASPR2), a multidomain transmembrane protein of the neurexin superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881352.RA2Tx9cYLvwPhoH43Q3tXVL-hPymCLxhDk4mrfYgs2JfQ130_provenance.
- NP881352.RA2Tx9cYLvwPhoH43Q3tXVL-hPymCLxhDk4mrfYgs2JfQ130_assertion evidence source_evidence_literature NP881352.RA2Tx9cYLvwPhoH43Q3tXVL-hPymCLxhDk4mrfYgs2JfQ130_provenance.
- NP881352.RA2Tx9cYLvwPhoH43Q3tXVL-hPymCLxhDk4mrfYgs2JfQ130_assertion SIO_000772 22872700 NP881352.RA2Tx9cYLvwPhoH43Q3tXVL-hPymCLxhDk4mrfYgs2JfQ130_provenance.
- NP881352.RA2Tx9cYLvwPhoH43Q3tXVL-hPymCLxhDk4mrfYgs2JfQ130_assertion wasDerivedFrom befree-20150227 NP881352.RA2Tx9cYLvwPhoH43Q3tXVL-hPymCLxhDk4mrfYgs2JfQ130_provenance.
- NP881352.RA2Tx9cYLvwPhoH43Q3tXVL-hPymCLxhDk4mrfYgs2JfQ130_assertion wasGeneratedBy ECO_0000203 NP881352.RA2Tx9cYLvwPhoH43Q3tXVL-hPymCLxhDk4mrfYgs2JfQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP881352.RA2Tx9cYLvwPhoH43Q3tXVL-hPymCLxhDk4mrfYgs2JfQ130_provenance.