Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978873.RAgA-W6F46Pu_fx8D8RueVkATwOosgpOhBpsq5wpFmC1k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978873.RAgA-W6F46Pu_fx8D8RueVkATwOosgpOhBpsq5wpFmC1k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978873.RAgA-W6F46Pu_fx8D8RueVkATwOosgpOhBpsq5wpFmC1k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978873.RAgA-W6F46Pu_fx8D8RueVkATwOosgpOhBpsq5wpFmC1k130_provenance.
- befree-2016 importedOn "2016-02-19" NP978873.RAgA-W6F46Pu_fx8D8RueVkATwOosgpOhBpsq5wpFmC1k130_provenance.
- NP978873.RAgA-W6F46Pu_fx8D8RueVkATwOosgpOhBpsq5wpFmC1k130_assertion wasGeneratedBy ECO_0000203 NP978873.RAgA-W6F46Pu_fx8D8RueVkATwOosgpOhBpsq5wpFmC1k130_provenance.
- NP978873.RAgA-W6F46Pu_fx8D8RueVkATwOosgpOhBpsq5wpFmC1k130_assertion wasDerivedFrom befree-2016 NP978873.RAgA-W6F46Pu_fx8D8RueVkATwOosgpOhBpsq5wpFmC1k130_provenance.
- NP978873.RAgA-W6F46Pu_fx8D8RueVkATwOosgpOhBpsq5wpFmC1k130_assertion SIO_000772 22549409 NP978873.RAgA-W6F46Pu_fx8D8RueVkATwOosgpOhBpsq5wpFmC1k130_provenance.
- NP978873.RAgA-W6F46Pu_fx8D8RueVkATwOosgpOhBpsq5wpFmC1k130_assertion evidence source_evidence_literature NP978873.RAgA-W6F46Pu_fx8D8RueVkATwOosgpOhBpsq5wpFmC1k130_provenance.
- NP978873.RAgA-W6F46Pu_fx8D8RueVkATwOosgpOhBpsq5wpFmC1k130_assertion description "[Clinical phenotype in POMT1-mutated patients ranges from congenital muscular dystrophy (CMD) with structural brain abnormalities, to limb-girdle muscular dystrophy (LGMD) with microcephaly and mental retardation, to mild LGMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978873.RAgA-W6F46Pu_fx8D8RueVkATwOosgpOhBpsq5wpFmC1k130_provenance.