Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583880.RAOpJ7AedPJDZsBrqkeMmje9F7mBl8qO4icEKWi39ViYg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583880.RAOpJ7AedPJDZsBrqkeMmje9F7mBl8qO4icEKWi39ViYg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583880.RAOpJ7AedPJDZsBrqkeMmje9F7mBl8qO4icEKWi39ViYg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583880.RAOpJ7AedPJDZsBrqkeMmje9F7mBl8qO4icEKWi39ViYg130_provenance.
- NP583880.RAOpJ7AedPJDZsBrqkeMmje9F7mBl8qO4icEKWi39ViYg130_assertion description "[We recently showed that some patients without MLC1 mutations display the classical phenotype; others improve or become normal but retain macrocephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583880.RAOpJ7AedPJDZsBrqkeMmje9F7mBl8qO4icEKWi39ViYg130_provenance.
- NP583880.RAOpJ7AedPJDZsBrqkeMmje9F7mBl8qO4icEKWi39ViYg130_assertion evidence source_evidence_literature NP583880.RAOpJ7AedPJDZsBrqkeMmje9F7mBl8qO4icEKWi39ViYg130_provenance.
- NP583880.RAOpJ7AedPJDZsBrqkeMmje9F7mBl8qO4icEKWi39ViYg130_assertion SIO_000772 21419380 NP583880.RAOpJ7AedPJDZsBrqkeMmje9F7mBl8qO4icEKWi39ViYg130_provenance.
- NP583880.RAOpJ7AedPJDZsBrqkeMmje9F7mBl8qO4icEKWi39ViYg130_assertion wasDerivedFrom befree-20150227 NP583880.RAOpJ7AedPJDZsBrqkeMmje9F7mBl8qO4icEKWi39ViYg130_provenance.
- NP583880.RAOpJ7AedPJDZsBrqkeMmje9F7mBl8qO4icEKWi39ViYg130_assertion wasGeneratedBy ECO_0000203 NP583880.RAOpJ7AedPJDZsBrqkeMmje9F7mBl8qO4icEKWi39ViYg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583880.RAOpJ7AedPJDZsBrqkeMmje9F7mBl8qO4icEKWi39ViYg130_provenance.