Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP719849.RAr5SOyUOYQ_Ltj3XV-6Qg2a-c7_Oj0r9AD8EZLOlhCVg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP719849.RAr5SOyUOYQ_Ltj3XV-6Qg2a-c7_Oj0r9AD8EZLOlhCVg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719849.RAr5SOyUOYQ_Ltj3XV-6Qg2a-c7_Oj0r9AD8EZLOlhCVg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719849.RAr5SOyUOYQ_Ltj3XV-6Qg2a-c7_Oj0r9AD8EZLOlhCVg130_provenance.
- NP719849.RAr5SOyUOYQ_Ltj3XV-6Qg2a-c7_Oj0r9AD8EZLOlhCVg130_assertion description "[We identified 12 patients with LWD who presented with a novel class of PAR1 deletions that did not include SHOX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719849.RAr5SOyUOYQ_Ltj3XV-6Qg2a-c7_Oj0r9AD8EZLOlhCVg130_provenance.
- NP719849.RAr5SOyUOYQ_Ltj3XV-6Qg2a-c7_Oj0r9AD8EZLOlhCVg130_assertion evidence source_evidence_literature NP719849.RAr5SOyUOYQ_Ltj3XV-6Qg2a-c7_Oj0r9AD8EZLOlhCVg130_provenance.
- NP719849.RAr5SOyUOYQ_Ltj3XV-6Qg2a-c7_Oj0r9AD8EZLOlhCVg130_assertion SIO_000772 16175500 NP719849.RAr5SOyUOYQ_Ltj3XV-6Qg2a-c7_Oj0r9AD8EZLOlhCVg130_provenance.
- NP719849.RAr5SOyUOYQ_Ltj3XV-6Qg2a-c7_Oj0r9AD8EZLOlhCVg130_assertion wasDerivedFrom befree-20140225 NP719849.RAr5SOyUOYQ_Ltj3XV-6Qg2a-c7_Oj0r9AD8EZLOlhCVg130_provenance.
- NP719849.RAr5SOyUOYQ_Ltj3XV-6Qg2a-c7_Oj0r9AD8EZLOlhCVg130_assertion wasGeneratedBy ECO_0000203 NP719849.RAr5SOyUOYQ_Ltj3XV-6Qg2a-c7_Oj0r9AD8EZLOlhCVg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP719849.RAr5SOyUOYQ_Ltj3XV-6Qg2a-c7_Oj0r9AD8EZLOlhCVg130_provenance.