Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP265694.RAq-wf9XZ0MXfxOrVAlXzzhBZpVHg1SSLulxAefmbTLZc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP265694.RAq-wf9XZ0MXfxOrVAlXzzhBZpVHg1SSLulxAefmbTLZc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP265694.RAq-wf9XZ0MXfxOrVAlXzzhBZpVHg1SSLulxAefmbTLZc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP265694.RAq-wf9XZ0MXfxOrVAlXzzhBZpVHg1SSLulxAefmbTLZc130_provenance.
- NP265694.RAq-wf9XZ0MXfxOrVAlXzzhBZpVHg1SSLulxAefmbTLZc130_assertion wasGeneratedBy ECO_0000203 NP265694.RAq-wf9XZ0MXfxOrVAlXzzhBZpVHg1SSLulxAefmbTLZc130_provenance.
- NP265694.RAq-wf9XZ0MXfxOrVAlXzzhBZpVHg1SSLulxAefmbTLZc130_assertion wasDerivedFrom befree-20140225 NP265694.RAq-wf9XZ0MXfxOrVAlXzzhBZpVHg1SSLulxAefmbTLZc130_provenance.
- NP265694.RAq-wf9XZ0MXfxOrVAlXzzhBZpVHg1SSLulxAefmbTLZc130_assertion SIO_000772 12467726 NP265694.RAq-wf9XZ0MXfxOrVAlXzzhBZpVHg1SSLulxAefmbTLZc130_provenance.
- NP265694.RAq-wf9XZ0MXfxOrVAlXzzhBZpVHg1SSLulxAefmbTLZc130_assertion evidence source_evidence_literature NP265694.RAq-wf9XZ0MXfxOrVAlXzzhBZpVHg1SSLulxAefmbTLZc130_provenance.
- NP265694.RAq-wf9XZ0MXfxOrVAlXzzhBZpVHg1SSLulxAefmbTLZc130_assertion description "[Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265694.RAq-wf9XZ0MXfxOrVAlXzzhBZpVHg1SSLulxAefmbTLZc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP265694.RAq-wf9XZ0MXfxOrVAlXzzhBZpVHg1SSLulxAefmbTLZc130_provenance.