Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP269205.RAA8iLHVyKp3I3pv3wdlNJMSVzw4v7iYwM5iFkd76MdDE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP269205.RAA8iLHVyKp3I3pv3wdlNJMSVzw4v7iYwM5iFkd76MdDE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP269205.RAA8iLHVyKp3I3pv3wdlNJMSVzw4v7iYwM5iFkd76MdDE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP269205.RAA8iLHVyKp3I3pv3wdlNJMSVzw4v7iYwM5iFkd76MdDE130_provenance.
- NP269205.RAA8iLHVyKp3I3pv3wdlNJMSVzw4v7iYwM5iFkd76MdDE130_assertion description "[A moderate increase in the number of PMP22 genes led to hypomyelination comparable to CMT1A, whereas high copy numbers of transgenic PMP22 resulted in phenotypes resembling more severe forms of hereditary motor and sensory neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269205.RAA8iLHVyKp3I3pv3wdlNJMSVzw4v7iYwM5iFkd76MdDE130_provenance.
- NP269205.RAA8iLHVyKp3I3pv3wdlNJMSVzw4v7iYwM5iFkd76MdDE130_assertion evidence source_evidence_literature NP269205.RAA8iLHVyKp3I3pv3wdlNJMSVzw4v7iYwM5iFkd76MdDE130_provenance.
- NP269205.RAA8iLHVyKp3I3pv3wdlNJMSVzw4v7iYwM5iFkd76MdDE130_assertion SIO_000772 10586249 NP269205.RAA8iLHVyKp3I3pv3wdlNJMSVzw4v7iYwM5iFkd76MdDE130_provenance.
- NP269205.RAA8iLHVyKp3I3pv3wdlNJMSVzw4v7iYwM5iFkd76MdDE130_assertion wasDerivedFrom befree-2016 NP269205.RAA8iLHVyKp3I3pv3wdlNJMSVzw4v7iYwM5iFkd76MdDE130_provenance.
- NP269205.RAA8iLHVyKp3I3pv3wdlNJMSVzw4v7iYwM5iFkd76MdDE130_assertion wasGeneratedBy ECO_0000203 NP269205.RAA8iLHVyKp3I3pv3wdlNJMSVzw4v7iYwM5iFkd76MdDE130_provenance.
- befree-2016 importedOn "2016-02-19" NP269205.RAA8iLHVyKp3I3pv3wdlNJMSVzw4v7iYwM5iFkd76MdDE130_provenance.