Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP175637.RAuSOWDB2yDVp61URZ4UALn2kipbsnxEvENtCOwvgdgL4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP175637.RAuSOWDB2yDVp61URZ4UALn2kipbsnxEvENtCOwvgdgL4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP175637.RAuSOWDB2yDVp61URZ4UALn2kipbsnxEvENtCOwvgdgL4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP175637.RAuSOWDB2yDVp61URZ4UALn2kipbsnxEvENtCOwvgdgL4130_provenance.
- NP175637.RAuSOWDB2yDVp61URZ4UALn2kipbsnxEvENtCOwvgdgL4130_assertion description "[Furthermore, we demonstrated that a ZFN pair could induce the inversion of a 140-kbp chromosomal segment that contains a portion of the blood coagulation factor VIII gene to mimic the inversion genotype that is associated with some cases of severe hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP175637.RAuSOWDB2yDVp61URZ4UALn2kipbsnxEvENtCOwvgdgL4130_provenance.
- NP175637.RAuSOWDB2yDVp61URZ4UALn2kipbsnxEvENtCOwvgdgL4130_assertion evidence source_evidence_literature NP175637.RAuSOWDB2yDVp61URZ4UALn2kipbsnxEvENtCOwvgdgL4130_provenance.
- NP175637.RAuSOWDB2yDVp61URZ4UALn2kipbsnxEvENtCOwvgdgL4130_assertion SIO_000772 22183967 NP175637.RAuSOWDB2yDVp61URZ4UALn2kipbsnxEvENtCOwvgdgL4130_provenance.
- NP175637.RAuSOWDB2yDVp61URZ4UALn2kipbsnxEvENtCOwvgdgL4130_assertion wasDerivedFrom befree-20140225 NP175637.RAuSOWDB2yDVp61URZ4UALn2kipbsnxEvENtCOwvgdgL4130_provenance.
- NP175637.RAuSOWDB2yDVp61URZ4UALn2kipbsnxEvENtCOwvgdgL4130_assertion wasGeneratedBy ECO_0000203 NP175637.RAuSOWDB2yDVp61URZ4UALn2kipbsnxEvENtCOwvgdgL4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP175637.RAuSOWDB2yDVp61URZ4UALn2kipbsnxEvENtCOwvgdgL4130_provenance.