Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_provenance.
- NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_assertion description "[The Spanish cohort, the largest group of patients studied so far, shares phenotypic features with both LGMD1A and MFM/MYOT variants thus establishing a continuum of phenotypic manifestations characteristic of myotilinopathy, an emerging neuromuscular disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_provenance.
- NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_assertion evidence source_evidence_literature NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_provenance.
- NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_assertion SIO_000772 15947064 NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_provenance.
- NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_assertion wasDerivedFrom befree-20140225 NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_provenance.
- NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_assertion wasGeneratedBy ECO_0000203 NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_provenance.