Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP631403.RAnIAIa7l4BCWbOGmaxyz1XjmYHW5qfKKR10NfI0h1Tow130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP631403.RAnIAIa7l4BCWbOGmaxyz1XjmYHW5qfKKR10NfI0h1Tow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP631403.RAnIAIa7l4BCWbOGmaxyz1XjmYHW5qfKKR10NfI0h1Tow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP631403.RAnIAIa7l4BCWbOGmaxyz1XjmYHW5qfKKR10NfI0h1Tow130_provenance.
- NP631403.RAnIAIa7l4BCWbOGmaxyz1XjmYHW5qfKKR10NfI0h1Tow130_assertion description "[Mutations of PLP1/DM20 cause Pelizaeus-Merzbacher Disease (PMD), a leukodystrophy, and in some instances, a peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631403.RAnIAIa7l4BCWbOGmaxyz1XjmYHW5qfKKR10NfI0h1Tow130_provenance.
- NP631403.RAnIAIa7l4BCWbOGmaxyz1XjmYHW5qfKKR10NfI0h1Tow130_assertion evidence source_evidence_literature NP631403.RAnIAIa7l4BCWbOGmaxyz1XjmYHW5qfKKR10NfI0h1Tow130_provenance.
- NP631403.RAnIAIa7l4BCWbOGmaxyz1XjmYHW5qfKKR10NfI0h1Tow130_assertion SIO_000772 12601703 NP631403.RAnIAIa7l4BCWbOGmaxyz1XjmYHW5qfKKR10NfI0h1Tow130_provenance.
- NP631403.RAnIAIa7l4BCWbOGmaxyz1XjmYHW5qfKKR10NfI0h1Tow130_assertion wasDerivedFrom befree-20150227 NP631403.RAnIAIa7l4BCWbOGmaxyz1XjmYHW5qfKKR10NfI0h1Tow130_provenance.
- NP631403.RAnIAIa7l4BCWbOGmaxyz1XjmYHW5qfKKR10NfI0h1Tow130_assertion wasGeneratedBy ECO_0000203 NP631403.RAnIAIa7l4BCWbOGmaxyz1XjmYHW5qfKKR10NfI0h1Tow130_provenance.
- befree-20150227 importedOn "2015-02-27" NP631403.RAnIAIa7l4BCWbOGmaxyz1XjmYHW5qfKKR10NfI0h1Tow130_provenance.