Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_provenance.
- NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_assertion description "[All patients with POMT1 and POMT2 mutations had evidence of either structural or functional central nervous system involvement including four patients with mental retardation and a LGMD phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_provenance.
- NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_assertion evidence source_evidence_literature NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_provenance.
- NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_assertion SIO_000772 17878207 NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_provenance.
- NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_assertion wasDerivedFrom befree-20150227 NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_provenance.
- NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_assertion wasGeneratedBy ECO_0000203 NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP895092.RAUVSnRWHP7GKZ1Ff6TX2LFgDdIE-aOHFuwMGPZ8-9q1g130_provenance.