Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP626584.RAkxXHwmQxqcIkhY0qJo3H0KfBy_0QheQr2oIjjeX7WTQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP626584.RAkxXHwmQxqcIkhY0qJo3H0KfBy_0QheQr2oIjjeX7WTQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626584.RAkxXHwmQxqcIkhY0qJo3H0KfBy_0QheQr2oIjjeX7WTQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626584.RAkxXHwmQxqcIkhY0qJo3H0KfBy_0QheQr2oIjjeX7WTQ130_provenance.
- NP626584.RAkxXHwmQxqcIkhY0qJo3H0KfBy_0QheQr2oIjjeX7WTQ130_assertion description "[Heterozygous and homozygous mutations in PITX3 in a large Lebanese family with posterior polar cataracts and neurodevelopmental abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626584.RAkxXHwmQxqcIkhY0qJo3H0KfBy_0QheQr2oIjjeX7WTQ130_provenance.
- NP626584.RAkxXHwmQxqcIkhY0qJo3H0KfBy_0QheQr2oIjjeX7WTQ130_assertion evidence source_evidence_literature NP626584.RAkxXHwmQxqcIkhY0qJo3H0KfBy_0QheQr2oIjjeX7WTQ130_provenance.
- NP626584.RAkxXHwmQxqcIkhY0qJo3H0KfBy_0QheQr2oIjjeX7WTQ130_assertion SIO_000772 16565358 NP626584.RAkxXHwmQxqcIkhY0qJo3H0KfBy_0QheQr2oIjjeX7WTQ130_provenance.
- NP626584.RAkxXHwmQxqcIkhY0qJo3H0KfBy_0QheQr2oIjjeX7WTQ130_assertion wasDerivedFrom befree-20150227 NP626584.RAkxXHwmQxqcIkhY0qJo3H0KfBy_0QheQr2oIjjeX7WTQ130_provenance.
- NP626584.RAkxXHwmQxqcIkhY0qJo3H0KfBy_0QheQr2oIjjeX7WTQ130_assertion wasGeneratedBy ECO_0000203 NP626584.RAkxXHwmQxqcIkhY0qJo3H0KfBy_0QheQr2oIjjeX7WTQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP626584.RAkxXHwmQxqcIkhY0qJo3H0KfBy_0QheQr2oIjjeX7WTQ130_provenance.