Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP782441.RAaLwxqMFfPAQ8FG38aF7cDi8LcKSwfxyOC48HDI0JHPY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP782441.RAaLwxqMFfPAQ8FG38aF7cDi8LcKSwfxyOC48HDI0JHPY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP782441.RAaLwxqMFfPAQ8FG38aF7cDi8LcKSwfxyOC48HDI0JHPY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP782441.RAaLwxqMFfPAQ8FG38aF7cDi8LcKSwfxyOC48HDI0JHPY130_provenance.
- NP782441.RAaLwxqMFfPAQ8FG38aF7cDi8LcKSwfxyOC48HDI0JHPY130_assertion description "[In this work, we reveal a novel insertion mutation in the 3'UTR of the FOXL2 gene in a big Chinese family which is to our knowledge the first BPES (type II) family reported in China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782441.RAaLwxqMFfPAQ8FG38aF7cDi8LcKSwfxyOC48HDI0JHPY130_provenance.
- NP782441.RAaLwxqMFfPAQ8FG38aF7cDi8LcKSwfxyOC48HDI0JHPY130_assertion evidence source_evidence_literature NP782441.RAaLwxqMFfPAQ8FG38aF7cDi8LcKSwfxyOC48HDI0JHPY130_provenance.
- NP782441.RAaLwxqMFfPAQ8FG38aF7cDi8LcKSwfxyOC48HDI0JHPY130_assertion SIO_000772 15450400 NP782441.RAaLwxqMFfPAQ8FG38aF7cDi8LcKSwfxyOC48HDI0JHPY130_provenance.
- NP782441.RAaLwxqMFfPAQ8FG38aF7cDi8LcKSwfxyOC48HDI0JHPY130_assertion wasDerivedFrom befree-20140225 NP782441.RAaLwxqMFfPAQ8FG38aF7cDi8LcKSwfxyOC48HDI0JHPY130_provenance.
- NP782441.RAaLwxqMFfPAQ8FG38aF7cDi8LcKSwfxyOC48HDI0JHPY130_assertion wasGeneratedBy ECO_0000203 NP782441.RAaLwxqMFfPAQ8FG38aF7cDi8LcKSwfxyOC48HDI0JHPY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP782441.RAaLwxqMFfPAQ8FG38aF7cDi8LcKSwfxyOC48HDI0JHPY130_provenance.