Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP558363.RA_j0ouzzWjQp4C5sQykRckAIMsVyfcj7tlLR8SZ4g1gU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP558363.RA_j0ouzzWjQp4C5sQykRckAIMsVyfcj7tlLR8SZ4g1gU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP558363.RA_j0ouzzWjQp4C5sQykRckAIMsVyfcj7tlLR8SZ4g1gU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP558363.RA_j0ouzzWjQp4C5sQykRckAIMsVyfcj7tlLR8SZ4g1gU130_provenance.
- NP558363.RA_j0ouzzWjQp4C5sQykRckAIMsVyfcj7tlLR8SZ4g1gU130_assertion description "[Recently, missense and truncating mutations in the gene PCDH19 have been reported to cause female-restricted epilepsy with mental retardation (EFMR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558363.RA_j0ouzzWjQp4C5sQykRckAIMsVyfcj7tlLR8SZ4g1gU130_provenance.
- NP558363.RA_j0ouzzWjQp4C5sQykRckAIMsVyfcj7tlLR8SZ4g1gU130_assertion evidence source_evidence_literature NP558363.RA_j0ouzzWjQp4C5sQykRckAIMsVyfcj7tlLR8SZ4g1gU130_provenance.
- NP558363.RA_j0ouzzWjQp4C5sQykRckAIMsVyfcj7tlLR8SZ4g1gU130_assertion SIO_000772 22091964 NP558363.RA_j0ouzzWjQp4C5sQykRckAIMsVyfcj7tlLR8SZ4g1gU130_provenance.
- NP558363.RA_j0ouzzWjQp4C5sQykRckAIMsVyfcj7tlLR8SZ4g1gU130_assertion wasDerivedFrom befree-20140225 NP558363.RA_j0ouzzWjQp4C5sQykRckAIMsVyfcj7tlLR8SZ4g1gU130_provenance.
- NP558363.RA_j0ouzzWjQp4C5sQykRckAIMsVyfcj7tlLR8SZ4g1gU130_assertion wasGeneratedBy ECO_0000203 NP558363.RA_j0ouzzWjQp4C5sQykRckAIMsVyfcj7tlLR8SZ4g1gU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP558363.RA_j0ouzzWjQp4C5sQykRckAIMsVyfcj7tlLR8SZ4g1gU130_provenance.