Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP885577.RAg5_pXgMBNvuL4EBJz2EargzKqoIwjB2d3QUes3__Z28130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP885577.RAg5_pXgMBNvuL4EBJz2EargzKqoIwjB2d3QUes3__Z28130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP885577.RAg5_pXgMBNvuL4EBJz2EargzKqoIwjB2d3QUes3__Z28130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP885577.RAg5_pXgMBNvuL4EBJz2EargzKqoIwjB2d3QUes3__Z28130_provenance.
- NP885577.RAg5_pXgMBNvuL4EBJz2EargzKqoIwjB2d3QUes3__Z28130_assertion description "[FOXP2 mutation causes a severe inherited speech and language defect, while the related transcription factors FOXP1, FOXP3 and FOXP4 are implicated in cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP885577.RAg5_pXgMBNvuL4EBJz2EargzKqoIwjB2d3QUes3__Z28130_provenance.
- NP885577.RAg5_pXgMBNvuL4EBJz2EargzKqoIwjB2d3QUes3__Z28130_assertion evidence source_evidence_literature NP885577.RAg5_pXgMBNvuL4EBJz2EargzKqoIwjB2d3QUes3__Z28130_provenance.
- NP885577.RAg5_pXgMBNvuL4EBJz2EargzKqoIwjB2d3QUes3__Z28130_assertion SIO_000772 20096010 NP885577.RAg5_pXgMBNvuL4EBJz2EargzKqoIwjB2d3QUes3__Z28130_provenance.
- NP885577.RAg5_pXgMBNvuL4EBJz2EargzKqoIwjB2d3QUes3__Z28130_assertion wasDerivedFrom befree-20150227 NP885577.RAg5_pXgMBNvuL4EBJz2EargzKqoIwjB2d3QUes3__Z28130_provenance.
- NP885577.RAg5_pXgMBNvuL4EBJz2EargzKqoIwjB2d3QUes3__Z28130_assertion wasGeneratedBy ECO_0000203 NP885577.RAg5_pXgMBNvuL4EBJz2EargzKqoIwjB2d3QUes3__Z28130_provenance.
- befree-20150227 importedOn "2015-02-27" NP885577.RAg5_pXgMBNvuL4EBJz2EargzKqoIwjB2d3QUes3__Z28130_provenance.