Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1071279.RAoVgCDuv8umQMQmOpRSjjXPNkia3C8-EkDsCSJTTDtAg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1071279.RAoVgCDuv8umQMQmOpRSjjXPNkia3C8-EkDsCSJTTDtAg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1071279.RAoVgCDuv8umQMQmOpRSjjXPNkia3C8-EkDsCSJTTDtAg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1071279.RAoVgCDuv8umQMQmOpRSjjXPNkia3C8-EkDsCSJTTDtAg130_provenance.
- NP1071279.RAoVgCDuv8umQMQmOpRSjjXPNkia3C8-EkDsCSJTTDtAg130_assertion description "[While four genes have been found to cause over 90�% of genetically identifiable causes of CMT (PMP22, GJB1, MPZ, MFN2), at least 51 genes and loci have been found to cause CMT when mutated, creating difficulties for clinicians to find a genetic subtype for families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1071279.RAoVgCDuv8umQMQmOpRSjjXPNkia3C8-EkDsCSJTTDtAg130_provenance.
- NP1071279.RAoVgCDuv8umQMQmOpRSjjXPNkia3C8-EkDsCSJTTDtAg130_assertion evidence source_evidence_literature NP1071279.RAoVgCDuv8umQMQmOpRSjjXPNkia3C8-EkDsCSJTTDtAg130_provenance.
- NP1071279.RAoVgCDuv8umQMQmOpRSjjXPNkia3C8-EkDsCSJTTDtAg130_assertion SIO_000772 23604902 NP1071279.RAoVgCDuv8umQMQmOpRSjjXPNkia3C8-EkDsCSJTTDtAg130_provenance.
- NP1071279.RAoVgCDuv8umQMQmOpRSjjXPNkia3C8-EkDsCSJTTDtAg130_assertion wasDerivedFrom befree-2016 NP1071279.RAoVgCDuv8umQMQmOpRSjjXPNkia3C8-EkDsCSJTTDtAg130_provenance.
- NP1071279.RAoVgCDuv8umQMQmOpRSjjXPNkia3C8-EkDsCSJTTDtAg130_assertion wasGeneratedBy ECO_0000203 NP1071279.RAoVgCDuv8umQMQmOpRSjjXPNkia3C8-EkDsCSJTTDtAg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1071279.RAoVgCDuv8umQMQmOpRSjjXPNkia3C8-EkDsCSJTTDtAg130_provenance.