Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_provenance.
- NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_assertion wasGeneratedBy ECO_0000203 NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_provenance.
- NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_assertion wasDerivedFrom befree-20150227 NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_provenance.
- NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_assertion SIO_000772 23228431 NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_provenance.
- NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_assertion evidence source_evidence_literature NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_provenance.
- NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881289.RA_eCvJyZo0HyHJ167Sou-UNQaC2KTPKuo4sXOE5RveTU130_provenance.