Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP635725.RAbrnxNECu-QVVsKNPLGpCyhGtttA6FFR0R1PRBTE-mbo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP635725.RAbrnxNECu-QVVsKNPLGpCyhGtttA6FFR0R1PRBTE-mbo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635725.RAbrnxNECu-QVVsKNPLGpCyhGtttA6FFR0R1PRBTE-mbo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635725.RAbrnxNECu-QVVsKNPLGpCyhGtttA6FFR0R1PRBTE-mbo130_provenance.
- NP635725.RAbrnxNECu-QVVsKNPLGpCyhGtttA6FFR0R1PRBTE-mbo130_assertion description "[OTX2 mutation in a patient with anophthalmia, short stature, and partial growth hormone deficiency: functional studies using the IRBP, HESX1, and POU1F1 promoters.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635725.RAbrnxNECu-QVVsKNPLGpCyhGtttA6FFR0R1PRBTE-mbo130_provenance.
- NP635725.RAbrnxNECu-QVVsKNPLGpCyhGtttA6FFR0R1PRBTE-mbo130_assertion evidence source_evidence_literature NP635725.RAbrnxNECu-QVVsKNPLGpCyhGtttA6FFR0R1PRBTE-mbo130_provenance.
- NP635725.RAbrnxNECu-QVVsKNPLGpCyhGtttA6FFR0R1PRBTE-mbo130_assertion SIO_000772 18628516 NP635725.RAbrnxNECu-QVVsKNPLGpCyhGtttA6FFR0R1PRBTE-mbo130_provenance.
- NP635725.RAbrnxNECu-QVVsKNPLGpCyhGtttA6FFR0R1PRBTE-mbo130_assertion wasDerivedFrom befree-20140225 NP635725.RAbrnxNECu-QVVsKNPLGpCyhGtttA6FFR0R1PRBTE-mbo130_provenance.
- NP635725.RAbrnxNECu-QVVsKNPLGpCyhGtttA6FFR0R1PRBTE-mbo130_assertion wasGeneratedBy ECO_0000203 NP635725.RAbrnxNECu-QVVsKNPLGpCyhGtttA6FFR0R1PRBTE-mbo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP635725.RAbrnxNECu-QVVsKNPLGpCyhGtttA6FFR0R1PRBTE-mbo130_provenance.