Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP741384.RAqaLIdlvkZaCq-cavL_eLztbbUx7xM4WIiXb7XSXc3k4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP741384.RAqaLIdlvkZaCq-cavL_eLztbbUx7xM4WIiXb7XSXc3k4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP741384.RAqaLIdlvkZaCq-cavL_eLztbbUx7xM4WIiXb7XSXc3k4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP741384.RAqaLIdlvkZaCq-cavL_eLztbbUx7xM4WIiXb7XSXc3k4130_provenance.
- NP741384.RAqaLIdlvkZaCq-cavL_eLztbbUx7xM4WIiXb7XSXc3k4130_assertion description "[These results indicate that the SRJ domain is dispensable for these functions of CITED2 in mice and that mutations clustering in the SRJ region are unlikely to be the sole cause of the malformations observed in patients with sporadic CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP741384.RAqaLIdlvkZaCq-cavL_eLztbbUx7xM4WIiXb7XSXc3k4130_provenance.
- NP741384.RAqaLIdlvkZaCq-cavL_eLztbbUx7xM4WIiXb7XSXc3k4130_assertion evidence source_evidence_literature NP741384.RAqaLIdlvkZaCq-cavL_eLztbbUx7xM4WIiXb7XSXc3k4130_provenance.
- NP741384.RAqaLIdlvkZaCq-cavL_eLztbbUx7xM4WIiXb7XSXc3k4130_assertion SIO_000772 23082118 NP741384.RAqaLIdlvkZaCq-cavL_eLztbbUx7xM4WIiXb7XSXc3k4130_provenance.
- NP741384.RAqaLIdlvkZaCq-cavL_eLztbbUx7xM4WIiXb7XSXc3k4130_assertion wasDerivedFrom befree-20140225 NP741384.RAqaLIdlvkZaCq-cavL_eLztbbUx7xM4WIiXb7XSXc3k4130_provenance.
- NP741384.RAqaLIdlvkZaCq-cavL_eLztbbUx7xM4WIiXb7XSXc3k4130_assertion wasGeneratedBy ECO_0000203 NP741384.RAqaLIdlvkZaCq-cavL_eLztbbUx7xM4WIiXb7XSXc3k4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP741384.RAqaLIdlvkZaCq-cavL_eLztbbUx7xM4WIiXb7XSXc3k4130_provenance.