Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1405561.RAQ7sAdEqQgl7VC0ZIjzPoXZsOPsAxMOdEA3o54GtdwqY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1405561.RAQ7sAdEqQgl7VC0ZIjzPoXZsOPsAxMOdEA3o54GtdwqY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1405561.RAQ7sAdEqQgl7VC0ZIjzPoXZsOPsAxMOdEA3o54GtdwqY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1405561.RAQ7sAdEqQgl7VC0ZIjzPoXZsOPsAxMOdEA3o54GtdwqY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1405561.RAQ7sAdEqQgl7VC0ZIjzPoXZsOPsAxMOdEA3o54GtdwqY130_provenance.
- NP1405561.RAQ7sAdEqQgl7VC0ZIjzPoXZsOPsAxMOdEA3o54GtdwqY130_assertion wasGeneratedBy ECO_0000203 NP1405561.RAQ7sAdEqQgl7VC0ZIjzPoXZsOPsAxMOdEA3o54GtdwqY130_provenance.
- NP1405561.RAQ7sAdEqQgl7VC0ZIjzPoXZsOPsAxMOdEA3o54GtdwqY130_assertion wasDerivedFrom befree-2016 NP1405561.RAQ7sAdEqQgl7VC0ZIjzPoXZsOPsAxMOdEA3o54GtdwqY130_provenance.
- NP1405561.RAQ7sAdEqQgl7VC0ZIjzPoXZsOPsAxMOdEA3o54GtdwqY130_assertion SIO_000772 9767294 NP1405561.RAQ7sAdEqQgl7VC0ZIjzPoXZsOPsAxMOdEA3o54GtdwqY130_provenance.
- NP1405561.RAQ7sAdEqQgl7VC0ZIjzPoXZsOPsAxMOdEA3o54GtdwqY130_assertion evidence source_evidence_literature NP1405561.RAQ7sAdEqQgl7VC0ZIjzPoXZsOPsAxMOdEA3o54GtdwqY130_provenance.
- NP1405561.RAQ7sAdEqQgl7VC0ZIjzPoXZsOPsAxMOdEA3o54GtdwqY130_assertion description "[Previously, we have demonstrated that PC-2 is caused by mutations in K17 and that similar mutations in this gene can present as steatocystoma multiplex with little or no nail dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1405561.RAQ7sAdEqQgl7VC0ZIjzPoXZsOPsAxMOdEA3o54GtdwqY130_provenance.