Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP450330.RAKF0v1vnBCr9lKoKZP1tUGgAhH43b7U3CEBr87hnC_qo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP450330.RAKF0v1vnBCr9lKoKZP1tUGgAhH43b7U3CEBr87hnC_qo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP450330.RAKF0v1vnBCr9lKoKZP1tUGgAhH43b7U3CEBr87hnC_qo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP450330.RAKF0v1vnBCr9lKoKZP1tUGgAhH43b7U3CEBr87hnC_qo130_provenance.
- NP450330.RAKF0v1vnBCr9lKoKZP1tUGgAhH43b7U3CEBr87hnC_qo130_assertion description "[We studied the PRRX1 gene in a non-consanguineous Indonesian female infant who was diagnosed prenatally with severe retrognathia (bilateral Pruzansky type III).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450330.RAKF0v1vnBCr9lKoKZP1tUGgAhH43b7U3CEBr87hnC_qo130_provenance.
- NP450330.RAKF0v1vnBCr9lKoKZP1tUGgAhH43b7U3CEBr87hnC_qo130_assertion evidence source_evidence_literature NP450330.RAKF0v1vnBCr9lKoKZP1tUGgAhH43b7U3CEBr87hnC_qo130_provenance.
- NP450330.RAKF0v1vnBCr9lKoKZP1tUGgAhH43b7U3CEBr87hnC_qo130_assertion SIO_000772 23444262 NP450330.RAKF0v1vnBCr9lKoKZP1tUGgAhH43b7U3CEBr87hnC_qo130_provenance.
- NP450330.RAKF0v1vnBCr9lKoKZP1tUGgAhH43b7U3CEBr87hnC_qo130_assertion wasDerivedFrom befree-20140225 NP450330.RAKF0v1vnBCr9lKoKZP1tUGgAhH43b7U3CEBr87hnC_qo130_provenance.
- NP450330.RAKF0v1vnBCr9lKoKZP1tUGgAhH43b7U3CEBr87hnC_qo130_assertion wasGeneratedBy ECO_0000203 NP450330.RAKF0v1vnBCr9lKoKZP1tUGgAhH43b7U3CEBr87hnC_qo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP450330.RAKF0v1vnBCr9lKoKZP1tUGgAhH43b7U3CEBr87hnC_qo130_provenance.