Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_provenance.
- NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_provenance.
- NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_assertion evidence source_evidence_literature NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_provenance.
- NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_assertion SIO_000772 18663734 NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_provenance.
- NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_assertion wasDerivedFrom befree-20140225 NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_provenance.
- NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_assertion wasGeneratedBy ECO_0000203 NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_provenance.