Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP630801.RA-lpS20lnXO2Cz-cbmk_wQN67vmCBfqNAYgiGiq4MCXI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP630801.RA-lpS20lnXO2Cz-cbmk_wQN67vmCBfqNAYgiGiq4MCXI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP630801.RA-lpS20lnXO2Cz-cbmk_wQN67vmCBfqNAYgiGiq4MCXI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP630801.RA-lpS20lnXO2Cz-cbmk_wQN67vmCBfqNAYgiGiq4MCXI130_provenance.
- NP630801.RA-lpS20lnXO2Cz-cbmk_wQN67vmCBfqNAYgiGiq4MCXI130_assertion description "[This study was conducted to report a family affected by benign hereditary chorea in which a large deletion including TTF1, PAX9, and other genes was identified and results in oligodontia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630801.RA-lpS20lnXO2Cz-cbmk_wQN67vmCBfqNAYgiGiq4MCXI130_provenance.
- NP630801.RA-lpS20lnXO2Cz-cbmk_wQN67vmCBfqNAYgiGiq4MCXI130_assertion evidence source_evidence_literature NP630801.RA-lpS20lnXO2Cz-cbmk_wQN67vmCBfqNAYgiGiq4MCXI130_provenance.
- NP630801.RA-lpS20lnXO2Cz-cbmk_wQN67vmCBfqNAYgiGiq4MCXI130_assertion SIO_000772 18445003 NP630801.RA-lpS20lnXO2Cz-cbmk_wQN67vmCBfqNAYgiGiq4MCXI130_provenance.
- NP630801.RA-lpS20lnXO2Cz-cbmk_wQN67vmCBfqNAYgiGiq4MCXI130_assertion wasDerivedFrom befree-20140225 NP630801.RA-lpS20lnXO2Cz-cbmk_wQN67vmCBfqNAYgiGiq4MCXI130_provenance.
- NP630801.RA-lpS20lnXO2Cz-cbmk_wQN67vmCBfqNAYgiGiq4MCXI130_assertion wasGeneratedBy ECO_0000203 NP630801.RA-lpS20lnXO2Cz-cbmk_wQN67vmCBfqNAYgiGiq4MCXI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP630801.RA-lpS20lnXO2Cz-cbmk_wQN67vmCBfqNAYgiGiq4MCXI130_provenance.