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- source_evidence_literature type ECO_0000212 NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_provenance.
- NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_assertion description "[Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_provenance.
- NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_assertion evidence source_evidence_literature NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_provenance.
- NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_assertion SIO_000772 23609221 NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_provenance.
- NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_assertion wasDerivedFrom befree-20150227 NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_provenance.
- NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_assertion wasGeneratedBy ECO_0000203 NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP357077.RAWhceYlZZaCeuR6YnmqSL4VK_1OVPw4SvvD-nEKj7l_A130_provenance.