Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP760770.RAJJ1tp9jk7ZFbYIFGTCIzCHn0os1hW6_q0QtR6ojJCFg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP760770.RAJJ1tp9jk7ZFbYIFGTCIzCHn0os1hW6_q0QtR6ojJCFg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP760770.RAJJ1tp9jk7ZFbYIFGTCIzCHn0os1hW6_q0QtR6ojJCFg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP760770.RAJJ1tp9jk7ZFbYIFGTCIzCHn0os1hW6_q0QtR6ojJCFg130_provenance.
- NP760770.RAJJ1tp9jk7ZFbYIFGTCIzCHn0os1hW6_q0QtR6ojJCFg130_assertion description "[While a role for SH3TC2, ADRB2, and HTR4 as putative candidate genes for autism cannot be discounted, a role for the desmocollin genes at the 18q breakpoint should also be considered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760770.RAJJ1tp9jk7ZFbYIFGTCIzCHn0os1hW6_q0QtR6ojJCFg130_provenance.
- NP760770.RAJJ1tp9jk7ZFbYIFGTCIzCHn0os1hW6_q0QtR6ojJCFg130_assertion evidence source_evidence_literature NP760770.RAJJ1tp9jk7ZFbYIFGTCIzCHn0os1hW6_q0QtR6ojJCFg130_provenance.
- NP760770.RAJJ1tp9jk7ZFbYIFGTCIzCHn0os1hW6_q0QtR6ojJCFg130_assertion SIO_000772 19086034 NP760770.RAJJ1tp9jk7ZFbYIFGTCIzCHn0os1hW6_q0QtR6ojJCFg130_provenance.
- NP760770.RAJJ1tp9jk7ZFbYIFGTCIzCHn0os1hW6_q0QtR6ojJCFg130_assertion wasDerivedFrom befree-20140225 NP760770.RAJJ1tp9jk7ZFbYIFGTCIzCHn0os1hW6_q0QtR6ojJCFg130_provenance.
- NP760770.RAJJ1tp9jk7ZFbYIFGTCIzCHn0os1hW6_q0QtR6ojJCFg130_assertion wasGeneratedBy ECO_0000203 NP760770.RAJJ1tp9jk7ZFbYIFGTCIzCHn0os1hW6_q0QtR6ojJCFg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP760770.RAJJ1tp9jk7ZFbYIFGTCIzCHn0os1hW6_q0QtR6ojJCFg130_provenance.