Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP715189.RA1PT_ZGh5oBVZFmuSZHD0P1SX4Owz4SAhR5GyKEfa46c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP715189.RA1PT_ZGh5oBVZFmuSZHD0P1SX4Owz4SAhR5GyKEfa46c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715189.RA1PT_ZGh5oBVZFmuSZHD0P1SX4Owz4SAhR5GyKEfa46c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715189.RA1PT_ZGh5oBVZFmuSZHD0P1SX4Owz4SAhR5GyKEfa46c130_provenance.
- NP715189.RA1PT_ZGh5oBVZFmuSZHD0P1SX4Owz4SAhR5GyKEfa46c130_assertion description "[NS, characterised by facial dysmorphism, congenital heart defects and short stature, is caused by mutations in the genes PTPN11, SOS1, KRAS and RAF1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715189.RA1PT_ZGh5oBVZFmuSZHD0P1SX4Owz4SAhR5GyKEfa46c130_provenance.
- NP715189.RA1PT_ZGh5oBVZFmuSZHD0P1SX4Owz4SAhR5GyKEfa46c130_assertion evidence source_evidence_literature NP715189.RA1PT_ZGh5oBVZFmuSZHD0P1SX4Owz4SAhR5GyKEfa46c130_provenance.
- NP715189.RA1PT_ZGh5oBVZFmuSZHD0P1SX4Owz4SAhR5GyKEfa46c130_assertion SIO_000772 18456719 NP715189.RA1PT_ZGh5oBVZFmuSZHD0P1SX4Owz4SAhR5GyKEfa46c130_provenance.
- NP715189.RA1PT_ZGh5oBVZFmuSZHD0P1SX4Owz4SAhR5GyKEfa46c130_assertion wasDerivedFrom befree-20140225 NP715189.RA1PT_ZGh5oBVZFmuSZHD0P1SX4Owz4SAhR5GyKEfa46c130_provenance.
- NP715189.RA1PT_ZGh5oBVZFmuSZHD0P1SX4Owz4SAhR5GyKEfa46c130_assertion wasGeneratedBy ECO_0000203 NP715189.RA1PT_ZGh5oBVZFmuSZHD0P1SX4Owz4SAhR5GyKEfa46c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP715189.RA1PT_ZGh5oBVZFmuSZHD0P1SX4Owz4SAhR5GyKEfa46c130_provenance.