Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP631241.RAAS4orsyuChziBYX7oFeUwWRRTG9X9xBYlGtzrO2-kEs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP631241.RAAS4orsyuChziBYX7oFeUwWRRTG9X9xBYlGtzrO2-kEs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP631241.RAAS4orsyuChziBYX7oFeUwWRRTG9X9xBYlGtzrO2-kEs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP631241.RAAS4orsyuChziBYX7oFeUwWRRTG9X9xBYlGtzrO2-kEs130_provenance.
- NP631241.RAAS4orsyuChziBYX7oFeUwWRRTG9X9xBYlGtzrO2-kEs130_assertion description "[Spastic paraplegia type 2 (SPG2) is allelic to Pelizaeus-Merzbacher disease (PMD), with both conditions resulting from mutations in the proteolipid protein gene (PLP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631241.RAAS4orsyuChziBYX7oFeUwWRRTG9X9xBYlGtzrO2-kEs130_provenance.
- NP631241.RAAS4orsyuChziBYX7oFeUwWRRTG9X9xBYlGtzrO2-kEs130_assertion evidence source_evidence_literature NP631241.RAAS4orsyuChziBYX7oFeUwWRRTG9X9xBYlGtzrO2-kEs130_provenance.
- NP631241.RAAS4orsyuChziBYX7oFeUwWRRTG9X9xBYlGtzrO2-kEs130_assertion SIO_000772 10319897 NP631241.RAAS4orsyuChziBYX7oFeUwWRRTG9X9xBYlGtzrO2-kEs130_provenance.
- NP631241.RAAS4orsyuChziBYX7oFeUwWRRTG9X9xBYlGtzrO2-kEs130_assertion wasDerivedFrom befree-20140225 NP631241.RAAS4orsyuChziBYX7oFeUwWRRTG9X9xBYlGtzrO2-kEs130_provenance.
- NP631241.RAAS4orsyuChziBYX7oFeUwWRRTG9X9xBYlGtzrO2-kEs130_assertion wasGeneratedBy ECO_0000203 NP631241.RAAS4orsyuChziBYX7oFeUwWRRTG9X9xBYlGtzrO2-kEs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP631241.RAAS4orsyuChziBYX7oFeUwWRRTG9X9xBYlGtzrO2-kEs130_provenance.