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- source_evidence_literature type ECO_0000212 NP601464.RA9DpKGzOU-M4hA8nG0YHIr9dkCYAQ2-VA9wjElxBcYw8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP601464.RA9DpKGzOU-M4hA8nG0YHIr9dkCYAQ2-VA9wjElxBcYw8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP601464.RA9DpKGzOU-M4hA8nG0YHIr9dkCYAQ2-VA9wjElxBcYw8130_provenance.
- NP601464.RA9DpKGzOU-M4hA8nG0YHIr9dkCYAQ2-VA9wjElxBcYw8130_assertion description "[The occuloalbinism 2 (OCA2) gene, localized at 15q11, encodes a melanosomal transmembrane protein that is involved in the most common form of human occulo-cutaneous albinism, a human genetic disorder characterized by fair pigmentation and susceptibility to skin cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601464.RA9DpKGzOU-M4hA8nG0YHIr9dkCYAQ2-VA9wjElxBcYw8130_provenance.
- NP601464.RA9DpKGzOU-M4hA8nG0YHIr9dkCYAQ2-VA9wjElxBcYw8130_assertion evidence source_evidence_literature NP601464.RA9DpKGzOU-M4hA8nG0YHIr9dkCYAQ2-VA9wjElxBcYw8130_provenance.
- NP601464.RA9DpKGzOU-M4hA8nG0YHIr9dkCYAQ2-VA9wjElxBcYw8130_assertion SIO_000772 15889046 NP601464.RA9DpKGzOU-M4hA8nG0YHIr9dkCYAQ2-VA9wjElxBcYw8130_provenance.
- NP601464.RA9DpKGzOU-M4hA8nG0YHIr9dkCYAQ2-VA9wjElxBcYw8130_assertion wasDerivedFrom befree-20150227 NP601464.RA9DpKGzOU-M4hA8nG0YHIr9dkCYAQ2-VA9wjElxBcYw8130_provenance.
- NP601464.RA9DpKGzOU-M4hA8nG0YHIr9dkCYAQ2-VA9wjElxBcYw8130_assertion wasGeneratedBy ECO_0000203 NP601464.RA9DpKGzOU-M4hA8nG0YHIr9dkCYAQ2-VA9wjElxBcYw8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP601464.RA9DpKGzOU-M4hA8nG0YHIr9dkCYAQ2-VA9wjElxBcYw8130_provenance.