Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP405589.RA6xf_qkVvbu0d_xf7rYuaU55vspZ4ZbfO31jaVnLX_QY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP405589.RA6xf_qkVvbu0d_xf7rYuaU55vspZ4ZbfO31jaVnLX_QY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP405589.RA6xf_qkVvbu0d_xf7rYuaU55vspZ4ZbfO31jaVnLX_QY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP405589.RA6xf_qkVvbu0d_xf7rYuaU55vspZ4ZbfO31jaVnLX_QY130_provenance.
- NP405589.RA6xf_qkVvbu0d_xf7rYuaU55vspZ4ZbfO31jaVnLX_QY130_assertion description "[Analogous to the putative perturbation of the anchoring function of the dystrophin-associated complex in congenital muscular dystrophy with mutations in the alpha 2-subunit of laminin, our observations suggest a similar mechanism in Bethlem myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP405589.RA6xf_qkVvbu0d_xf7rYuaU55vspZ4ZbfO31jaVnLX_QY130_provenance.
- NP405589.RA6xf_qkVvbu0d_xf7rYuaU55vspZ4ZbfO31jaVnLX_QY130_assertion evidence source_evidence_literature NP405589.RA6xf_qkVvbu0d_xf7rYuaU55vspZ4ZbfO31jaVnLX_QY130_provenance.
- NP405589.RA6xf_qkVvbu0d_xf7rYuaU55vspZ4ZbfO31jaVnLX_QY130_assertion SIO_000772 8782832 NP405589.RA6xf_qkVvbu0d_xf7rYuaU55vspZ4ZbfO31jaVnLX_QY130_provenance.
- NP405589.RA6xf_qkVvbu0d_xf7rYuaU55vspZ4ZbfO31jaVnLX_QY130_assertion wasDerivedFrom befree-20140225 NP405589.RA6xf_qkVvbu0d_xf7rYuaU55vspZ4ZbfO31jaVnLX_QY130_provenance.
- NP405589.RA6xf_qkVvbu0d_xf7rYuaU55vspZ4ZbfO31jaVnLX_QY130_assertion wasGeneratedBy ECO_0000203 NP405589.RA6xf_qkVvbu0d_xf7rYuaU55vspZ4ZbfO31jaVnLX_QY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP405589.RA6xf_qkVvbu0d_xf7rYuaU55vspZ4ZbfO31jaVnLX_QY130_provenance.