Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_provenance.
- NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_assertion description "[CMT1, an inherited motor and sensory neuropathy with low nerve conduction velocities, is caused by dominantly inherited mutations in the genes of the peripheral myelin protein 22 (PMP22), myelin protein zero (MPZ/P(0)), and early growth response 2 transcription factor (EGR2/Krox-20).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_provenance.
- NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_assertion evidence source_evidence_literature NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_provenance.
- NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_assertion SIO_000772 11445635 NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_provenance.
- NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_assertion wasDerivedFrom befree-2016 NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_provenance.
- NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_assertion wasGeneratedBy ECO_0000203 NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_provenance.
- befree-2016 importedOn "2016-02-19" NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_provenance.