Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP962603.RAoVQPmceJv5-8YAl-CLR5Vt_rszhNtborTLvvDJ1kfGw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP962603.RAoVQPmceJv5-8YAl-CLR5Vt_rszhNtborTLvvDJ1kfGw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP962603.RAoVQPmceJv5-8YAl-CLR5Vt_rszhNtborTLvvDJ1kfGw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP962603.RAoVQPmceJv5-8YAl-CLR5Vt_rszhNtborTLvvDJ1kfGw130_provenance.
- NP962603.RAoVQPmceJv5-8YAl-CLR5Vt_rszhNtborTLvvDJ1kfGw130_assertion description "[FOXP2 mutation causes a severe inherited speech and language defect, while the related transcription factors FOXP1, FOXP3 and FOXP4 are implicated in cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP962603.RAoVQPmceJv5-8YAl-CLR5Vt_rszhNtborTLvvDJ1kfGw130_provenance.
- NP962603.RAoVQPmceJv5-8YAl-CLR5Vt_rszhNtborTLvvDJ1kfGw130_assertion evidence source_evidence_literature NP962603.RAoVQPmceJv5-8YAl-CLR5Vt_rszhNtborTLvvDJ1kfGw130_provenance.
- NP962603.RAoVQPmceJv5-8YAl-CLR5Vt_rszhNtborTLvvDJ1kfGw130_assertion SIO_000772 20096010 NP962603.RAoVQPmceJv5-8YAl-CLR5Vt_rszhNtborTLvvDJ1kfGw130_provenance.
- NP962603.RAoVQPmceJv5-8YAl-CLR5Vt_rszhNtborTLvvDJ1kfGw130_assertion wasDerivedFrom befree-20150227 NP962603.RAoVQPmceJv5-8YAl-CLR5Vt_rszhNtborTLvvDJ1kfGw130_provenance.
- NP962603.RAoVQPmceJv5-8YAl-CLR5Vt_rszhNtborTLvvDJ1kfGw130_assertion wasGeneratedBy ECO_0000203 NP962603.RAoVQPmceJv5-8YAl-CLR5Vt_rszhNtborTLvvDJ1kfGw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP962603.RAoVQPmceJv5-8YAl-CLR5Vt_rszhNtborTLvvDJ1kfGw130_provenance.