Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP315464.RAwOLFWCNlxA3J8XBEki-GAzDHSUXlp-41NN_zD4C-r6Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP315464.RAwOLFWCNlxA3J8XBEki-GAzDHSUXlp-41NN_zD4C-r6Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP315464.RAwOLFWCNlxA3J8XBEki-GAzDHSUXlp-41NN_zD4C-r6Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP315464.RAwOLFWCNlxA3J8XBEki-GAzDHSUXlp-41NN_zD4C-r6Y130_provenance.
- NP315464.RAwOLFWCNlxA3J8XBEki-GAzDHSUXlp-41NN_zD4C-r6Y130_assertion description "[PITX2 mutations are known to be responsible for Axenfield Rieger syndrome, a genetic disorder in which pituitary abnormalities have been detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315464.RAwOLFWCNlxA3J8XBEki-GAzDHSUXlp-41NN_zD4C-r6Y130_provenance.
- NP315464.RAwOLFWCNlxA3J8XBEki-GAzDHSUXlp-41NN_zD4C-r6Y130_assertion evidence source_evidence_literature NP315464.RAwOLFWCNlxA3J8XBEki-GAzDHSUXlp-41NN_zD4C-r6Y130_provenance.
- NP315464.RAwOLFWCNlxA3J8XBEki-GAzDHSUXlp-41NN_zD4C-r6Y130_assertion SIO_000772 21810944 NP315464.RAwOLFWCNlxA3J8XBEki-GAzDHSUXlp-41NN_zD4C-r6Y130_provenance.
- NP315464.RAwOLFWCNlxA3J8XBEki-GAzDHSUXlp-41NN_zD4C-r6Y130_assertion wasDerivedFrom befree-20140225 NP315464.RAwOLFWCNlxA3J8XBEki-GAzDHSUXlp-41NN_zD4C-r6Y130_provenance.
- NP315464.RAwOLFWCNlxA3J8XBEki-GAzDHSUXlp-41NN_zD4C-r6Y130_assertion wasGeneratedBy ECO_0000203 NP315464.RAwOLFWCNlxA3J8XBEki-GAzDHSUXlp-41NN_zD4C-r6Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP315464.RAwOLFWCNlxA3J8XBEki-GAzDHSUXlp-41NN_zD4C-r6Y130_provenance.