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- source_evidence_literature type ECO_0000212 NP568253.RALBnrjZNuEn0zoU9itSe11DRwbzFv-XPmFewetZxbwGs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568253.RALBnrjZNuEn0zoU9itSe11DRwbzFv-XPmFewetZxbwGs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568253.RALBnrjZNuEn0zoU9itSe11DRwbzFv-XPmFewetZxbwGs130_provenance.
- NP568253.RALBnrjZNuEn0zoU9itSe11DRwbzFv-XPmFewetZxbwGs130_assertion description "[Myelin protein zero gene (MPZ) mutations usually cause a demyelinating variant of Charcot-Marie-Tooth disease type 1B (CMT1B), but there is a wide spectrum of phenotypic manifestation of these mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568253.RALBnrjZNuEn0zoU9itSe11DRwbzFv-XPmFewetZxbwGs130_provenance.
- NP568253.RALBnrjZNuEn0zoU9itSe11DRwbzFv-XPmFewetZxbwGs130_assertion evidence source_evidence_literature NP568253.RALBnrjZNuEn0zoU9itSe11DRwbzFv-XPmFewetZxbwGs130_provenance.
- NP568253.RALBnrjZNuEn0zoU9itSe11DRwbzFv-XPmFewetZxbwGs130_assertion SIO_000772 18663734 NP568253.RALBnrjZNuEn0zoU9itSe11DRwbzFv-XPmFewetZxbwGs130_provenance.
- NP568253.RALBnrjZNuEn0zoU9itSe11DRwbzFv-XPmFewetZxbwGs130_assertion wasDerivedFrom befree-20150227 NP568253.RALBnrjZNuEn0zoU9itSe11DRwbzFv-XPmFewetZxbwGs130_provenance.
- NP568253.RALBnrjZNuEn0zoU9itSe11DRwbzFv-XPmFewetZxbwGs130_assertion wasGeneratedBy ECO_0000203 NP568253.RALBnrjZNuEn0zoU9itSe11DRwbzFv-XPmFewetZxbwGs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568253.RALBnrjZNuEn0zoU9itSe11DRwbzFv-XPmFewetZxbwGs130_provenance.