Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP501326.RAchOWLQBAmnGt-GEdoHxPWXfPrbuayJYMpufTYnk8jwQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP501326.RAchOWLQBAmnGt-GEdoHxPWXfPrbuayJYMpufTYnk8jwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP501326.RAchOWLQBAmnGt-GEdoHxPWXfPrbuayJYMpufTYnk8jwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP501326.RAchOWLQBAmnGt-GEdoHxPWXfPrbuayJYMpufTYnk8jwQ130_provenance.
- NP501326.RAchOWLQBAmnGt-GEdoHxPWXfPrbuayJYMpufTYnk8jwQ130_assertion description "[The X-linked recessive centronuclear/myotubular myopathy (XLR-CNM/MTM1), a severe neonatal disorder characterized by generalized hypotonia, muscle weakness and primary asphyxia, has recently been mapped to Xq28.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP501326.RAchOWLQBAmnGt-GEdoHxPWXfPrbuayJYMpufTYnk8jwQ130_provenance.
- NP501326.RAchOWLQBAmnGt-GEdoHxPWXfPrbuayJYMpufTYnk8jwQ130_assertion evidence source_evidence_literature NP501326.RAchOWLQBAmnGt-GEdoHxPWXfPrbuayJYMpufTYnk8jwQ130_provenance.
- NP501326.RAchOWLQBAmnGt-GEdoHxPWXfPrbuayJYMpufTYnk8jwQ130_assertion SIO_000772 1822801 NP501326.RAchOWLQBAmnGt-GEdoHxPWXfPrbuayJYMpufTYnk8jwQ130_provenance.
- NP501326.RAchOWLQBAmnGt-GEdoHxPWXfPrbuayJYMpufTYnk8jwQ130_assertion wasDerivedFrom befree-20140225 NP501326.RAchOWLQBAmnGt-GEdoHxPWXfPrbuayJYMpufTYnk8jwQ130_provenance.
- NP501326.RAchOWLQBAmnGt-GEdoHxPWXfPrbuayJYMpufTYnk8jwQ130_assertion wasGeneratedBy ECO_0000203 NP501326.RAchOWLQBAmnGt-GEdoHxPWXfPrbuayJYMpufTYnk8jwQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP501326.RAchOWLQBAmnGt-GEdoHxPWXfPrbuayJYMpufTYnk8jwQ130_provenance.