Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP793897.RAYFcDGCoGxHcwHwJmQD5bQr74gG4iIe3JOVnwb8K5Ps4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP793897.RAYFcDGCoGxHcwHwJmQD5bQr74gG4iIe3JOVnwb8K5Ps4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP793897.RAYFcDGCoGxHcwHwJmQD5bQr74gG4iIe3JOVnwb8K5Ps4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP793897.RAYFcDGCoGxHcwHwJmQD5bQr74gG4iIe3JOVnwb8K5Ps4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP793897.RAYFcDGCoGxHcwHwJmQD5bQr74gG4iIe3JOVnwb8K5Ps4130_provenance.
- NP793897.RAYFcDGCoGxHcwHwJmQD5bQr74gG4iIe3JOVnwb8K5Ps4130_assertion wasGeneratedBy ECO_0000203 NP793897.RAYFcDGCoGxHcwHwJmQD5bQr74gG4iIe3JOVnwb8K5Ps4130_provenance.
- NP793897.RAYFcDGCoGxHcwHwJmQD5bQr74gG4iIe3JOVnwb8K5Ps4130_assertion wasDerivedFrom befree-20150227 NP793897.RAYFcDGCoGxHcwHwJmQD5bQr74gG4iIe3JOVnwb8K5Ps4130_provenance.
- NP793897.RAYFcDGCoGxHcwHwJmQD5bQr74gG4iIe3JOVnwb8K5Ps4130_assertion SIO_000772 22468107 NP793897.RAYFcDGCoGxHcwHwJmQD5bQr74gG4iIe3JOVnwb8K5Ps4130_provenance.
- NP793897.RAYFcDGCoGxHcwHwJmQD5bQr74gG4iIe3JOVnwb8K5Ps4130_assertion evidence source_evidence_literature NP793897.RAYFcDGCoGxHcwHwJmQD5bQr74gG4iIe3JOVnwb8K5Ps4130_provenance.
- NP793897.RAYFcDGCoGxHcwHwJmQD5bQr74gG4iIe3JOVnwb8K5Ps4130_assertion description "[The patients with dysferlinopathy were classified by initial muscle weakness: fifteen patients with Miyoshi myopathy phenotype (MM), thirteen patients with limb girdle muscular dystrophy 2B phenotype (LGMD2B), two patients with proximodistal phenotype, and one asymptomatic patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP793897.RAYFcDGCoGxHcwHwJmQD5bQr74gG4iIe3JOVnwb8K5Ps4130_provenance.