Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP876459.RAo9SJ0yGXmwm_jvkqPRaX6rNc22TRRGy2wMhDyJYXSQA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP876459.RAo9SJ0yGXmwm_jvkqPRaX6rNc22TRRGy2wMhDyJYXSQA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP876459.RAo9SJ0yGXmwm_jvkqPRaX6rNc22TRRGy2wMhDyJYXSQA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP876459.RAo9SJ0yGXmwm_jvkqPRaX6rNc22TRRGy2wMhDyJYXSQA130_provenance.
- NP876459.RAo9SJ0yGXmwm_jvkqPRaX6rNc22TRRGy2wMhDyJYXSQA130_assertion description "[Furthermore, we discuss possible explanations for the phenotypic differences between EEM and congenital hypotrichosis with juvenile macular dystrophy (HJMD), which is also caused by CDH3 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP876459.RAo9SJ0yGXmwm_jvkqPRaX6rNc22TRRGy2wMhDyJYXSQA130_provenance.
- NP876459.RAo9SJ0yGXmwm_jvkqPRaX6rNc22TRRGy2wMhDyJYXSQA130_assertion evidence source_evidence_literature NP876459.RAo9SJ0yGXmwm_jvkqPRaX6rNc22TRRGy2wMhDyJYXSQA130_provenance.
- NP876459.RAo9SJ0yGXmwm_jvkqPRaX6rNc22TRRGy2wMhDyJYXSQA130_assertion SIO_000772 15805154 NP876459.RAo9SJ0yGXmwm_jvkqPRaX6rNc22TRRGy2wMhDyJYXSQA130_provenance.
- NP876459.RAo9SJ0yGXmwm_jvkqPRaX6rNc22TRRGy2wMhDyJYXSQA130_assertion wasDerivedFrom befree-20140225 NP876459.RAo9SJ0yGXmwm_jvkqPRaX6rNc22TRRGy2wMhDyJYXSQA130_provenance.
- NP876459.RAo9SJ0yGXmwm_jvkqPRaX6rNc22TRRGy2wMhDyJYXSQA130_assertion wasGeneratedBy ECO_0000203 NP876459.RAo9SJ0yGXmwm_jvkqPRaX6rNc22TRRGy2wMhDyJYXSQA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP876459.RAo9SJ0yGXmwm_jvkqPRaX6rNc22TRRGy2wMhDyJYXSQA130_provenance.