Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_provenance.
- NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_assertion description "[Myotubularin (hMTM1), the founder member, is mutated in myotubular myopathy, and a close homolog (hMTMR2) was recently found mutated in a recessive form of Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_provenance.
- NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_assertion evidence source_evidence_literature NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_provenance.
- NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_assertion SIO_000772 11275328 NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_provenance.
- NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_assertion wasDerivedFrom befree-20140225 NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_provenance.
- NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_assertion wasGeneratedBy ECO_0000203 NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_provenance.