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- source_evidence_literature type ECO_0000212 NP1134420.RAJC6Y1u-3Bvxo5S1hxP8gHIHcX7Oh4VgUswlO4KvB5Ks130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1134420.RAJC6Y1u-3Bvxo5S1hxP8gHIHcX7Oh4VgUswlO4KvB5Ks130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1134420.RAJC6Y1u-3Bvxo5S1hxP8gHIHcX7Oh4VgUswlO4KvB5Ks130_provenance.
- befree-2016 importedOn "2016-02-19" NP1134420.RAJC6Y1u-3Bvxo5S1hxP8gHIHcX7Oh4VgUswlO4KvB5Ks130_provenance.
- NP1134420.RAJC6Y1u-3Bvxo5S1hxP8gHIHcX7Oh4VgUswlO4KvB5Ks130_assertion wasGeneratedBy ECO_0000203 NP1134420.RAJC6Y1u-3Bvxo5S1hxP8gHIHcX7Oh4VgUswlO4KvB5Ks130_provenance.
- NP1134420.RAJC6Y1u-3Bvxo5S1hxP8gHIHcX7Oh4VgUswlO4KvB5Ks130_assertion wasDerivedFrom befree-2016 NP1134420.RAJC6Y1u-3Bvxo5S1hxP8gHIHcX7Oh4VgUswlO4KvB5Ks130_provenance.
- NP1134420.RAJC6Y1u-3Bvxo5S1hxP8gHIHcX7Oh4VgUswlO4KvB5Ks130_assertion SIO_000772 24312213 NP1134420.RAJC6Y1u-3Bvxo5S1hxP8gHIHcX7Oh4VgUswlO4KvB5Ks130_provenance.
- NP1134420.RAJC6Y1u-3Bvxo5S1hxP8gHIHcX7Oh4VgUswlO4KvB5Ks130_assertion evidence source_evidence_literature NP1134420.RAJC6Y1u-3Bvxo5S1hxP8gHIHcX7Oh4VgUswlO4KvB5Ks130_provenance.
- NP1134420.RAJC6Y1u-3Bvxo5S1hxP8gHIHcX7Oh4VgUswlO4KvB5Ks130_assertion description "[Although WNT10A gene mutations are known to cause rare syndromes associated with tooth agenesis, including onycho-odontodermal dysplasia (OODD), Schöpf-Schulz-Passarge syndrome (SSPS), hypohidrotic ectodermal dysplasia (HED), and more than half of the cases of isolated oligodontia recently, the genotype-phenotype correlations and the mode of inheritance of WNT10A mutations remain unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1134420.RAJC6Y1u-3Bvxo5S1hxP8gHIHcX7Oh4VgUswlO4KvB5Ks130_provenance.