Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP612528.RAm36vW-uXb6LpkpUrW8fX89YCfmVUCP0nL9rgZXB7IHk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP612528.RAm36vW-uXb6LpkpUrW8fX89YCfmVUCP0nL9rgZXB7IHk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP612528.RAm36vW-uXb6LpkpUrW8fX89YCfmVUCP0nL9rgZXB7IHk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP612528.RAm36vW-uXb6LpkpUrW8fX89YCfmVUCP0nL9rgZXB7IHk130_provenance.
- NP612528.RAm36vW-uXb6LpkpUrW8fX89YCfmVUCP0nL9rgZXB7IHk130_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." NP612528.RAm36vW-uXb6LpkpUrW8fX89YCfmVUCP0nL9rgZXB7IHk130_provenance.
- NP612528.RAm36vW-uXb6LpkpUrW8fX89YCfmVUCP0nL9rgZXB7IHk130_assertion evidence source_evidence_literature NP612528.RAm36vW-uXb6LpkpUrW8fX89YCfmVUCP0nL9rgZXB7IHk130_provenance.
- NP612528.RAm36vW-uXb6LpkpUrW8fX89YCfmVUCP0nL9rgZXB7IHk130_assertion SIO_000772 15889046 NP612528.RAm36vW-uXb6LpkpUrW8fX89YCfmVUCP0nL9rgZXB7IHk130_provenance.
- NP612528.RAm36vW-uXb6LpkpUrW8fX89YCfmVUCP0nL9rgZXB7IHk130_assertion wasDerivedFrom befree-20140225 NP612528.RAm36vW-uXb6LpkpUrW8fX89YCfmVUCP0nL9rgZXB7IHk130_provenance.
- NP612528.RAm36vW-uXb6LpkpUrW8fX89YCfmVUCP0nL9rgZXB7IHk130_assertion wasGeneratedBy ECO_0000203 NP612528.RAm36vW-uXb6LpkpUrW8fX89YCfmVUCP0nL9rgZXB7IHk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP612528.RAm36vW-uXb6LpkpUrW8fX89YCfmVUCP0nL9rgZXB7IHk130_provenance.