Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP427754.RAqIL2kGp-Sm9CW089Jngg3Su_5ApUZwG5GTzKp7U_ooo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP427754.RAqIL2kGp-Sm9CW089Jngg3Su_5ApUZwG5GTzKp7U_ooo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP427754.RAqIL2kGp-Sm9CW089Jngg3Su_5ApUZwG5GTzKp7U_ooo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP427754.RAqIL2kGp-Sm9CW089Jngg3Su_5ApUZwG5GTzKp7U_ooo130_provenance.
- NP427754.RAqIL2kGp-Sm9CW089Jngg3Su_5ApUZwG5GTzKp7U_ooo130_assertion description "[Deletions and inactivating mutations of FOXG1 have been associated with a Rett-like syndrome characterized by hypotonia, irritability, developmental delay, hand stereotypies, and deceleration of head growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427754.RAqIL2kGp-Sm9CW089Jngg3Su_5ApUZwG5GTzKp7U_ooo130_provenance.
- NP427754.RAqIL2kGp-Sm9CW089Jngg3Su_5ApUZwG5GTzKp7U_ooo130_assertion evidence source_evidence_literature NP427754.RAqIL2kGp-Sm9CW089Jngg3Su_5ApUZwG5GTzKp7U_ooo130_provenance.
- NP427754.RAqIL2kGp-Sm9CW089Jngg3Su_5ApUZwG5GTzKp7U_ooo130_assertion SIO_000772 20736978 NP427754.RAqIL2kGp-Sm9CW089Jngg3Su_5ApUZwG5GTzKp7U_ooo130_provenance.
- NP427754.RAqIL2kGp-Sm9CW089Jngg3Su_5ApUZwG5GTzKp7U_ooo130_assertion wasDerivedFrom befree-20140225 NP427754.RAqIL2kGp-Sm9CW089Jngg3Su_5ApUZwG5GTzKp7U_ooo130_provenance.
- NP427754.RAqIL2kGp-Sm9CW089Jngg3Su_5ApUZwG5GTzKp7U_ooo130_assertion wasGeneratedBy ECO_0000203 NP427754.RAqIL2kGp-Sm9CW089Jngg3Su_5ApUZwG5GTzKp7U_ooo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP427754.RAqIL2kGp-Sm9CW089Jngg3Su_5ApUZwG5GTzKp7U_ooo130_provenance.