Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_provenance.
- NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_assertion description "[To further analyse the involvement of SHANK3 in ASD, we screened the International Molecular Genetic Study of Autism Consortium (IMGSAC) multiplex family sample, 330 families, for SNP association and copy number variants (CNVs) in SHANK3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_provenance.
- NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_assertion evidence source_evidence_literature NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_provenance.
- NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_assertion SIO_000772 19384346 NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_provenance.
- NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_assertion wasDerivedFrom befree-20140225 NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_provenance.
- NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_assertion wasGeneratedBy ECO_0000203 NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_provenance.