Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_provenance.
- NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_assertion description "[Mutations in the myotubularin (MTM)-related protein 2 (MTMR2) gene are responsible for the severe autosomal recessive neuropathy Charcot-Marie-Tooth disease type 4B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_provenance.
- NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_assertion evidence source_evidence_literature NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_provenance.
- NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_assertion SIO_000772 14530412 NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_provenance.
- NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_assertion wasDerivedFrom befree-20140225 NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_provenance.
- NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_assertion wasGeneratedBy ECO_0000203 NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_provenance.
- befree-20140225 importedOn "2014-02-25" NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_provenance.