Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP412633.RAWGGyLGbV37hJkoroDygz9ZMZRtScCKrnXTUPCp0qkKo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP412633.RAWGGyLGbV37hJkoroDygz9ZMZRtScCKrnXTUPCp0qkKo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412633.RAWGGyLGbV37hJkoroDygz9ZMZRtScCKrnXTUPCp0qkKo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412633.RAWGGyLGbV37hJkoroDygz9ZMZRtScCKrnXTUPCp0qkKo130_provenance.
- NP412633.RAWGGyLGbV37hJkoroDygz9ZMZRtScCKrnXTUPCp0qkKo130_assertion description "[Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412633.RAWGGyLGbV37hJkoroDygz9ZMZRtScCKrnXTUPCp0qkKo130_provenance.
- NP412633.RAWGGyLGbV37hJkoroDygz9ZMZRtScCKrnXTUPCp0qkKo130_assertion evidence source_evidence_literature NP412633.RAWGGyLGbV37hJkoroDygz9ZMZRtScCKrnXTUPCp0qkKo130_provenance.
- NP412633.RAWGGyLGbV37hJkoroDygz9ZMZRtScCKrnXTUPCp0qkKo130_assertion SIO_000772 23307483 NP412633.RAWGGyLGbV37hJkoroDygz9ZMZRtScCKrnXTUPCp0qkKo130_provenance.
- NP412633.RAWGGyLGbV37hJkoroDygz9ZMZRtScCKrnXTUPCp0qkKo130_assertion wasDerivedFrom befree-20150227 NP412633.RAWGGyLGbV37hJkoroDygz9ZMZRtScCKrnXTUPCp0qkKo130_provenance.
- NP412633.RAWGGyLGbV37hJkoroDygz9ZMZRtScCKrnXTUPCp0qkKo130_assertion wasGeneratedBy ECO_0000203 NP412633.RAWGGyLGbV37hJkoroDygz9ZMZRtScCKrnXTUPCp0qkKo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP412633.RAWGGyLGbV37hJkoroDygz9ZMZRtScCKrnXTUPCp0qkKo130_provenance.