Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP145422.RAxOskPvRKMLVKtjE2xHcu3tgw0h3k8gZkG15nSHMQZ1w130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP145422.RAxOskPvRKMLVKtjE2xHcu3tgw0h3k8gZkG15nSHMQZ1w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP145422.RAxOskPvRKMLVKtjE2xHcu3tgw0h3k8gZkG15nSHMQZ1w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP145422.RAxOskPvRKMLVKtjE2xHcu3tgw0h3k8gZkG15nSHMQZ1w130_provenance.
- NP145422.RAxOskPvRKMLVKtjE2xHcu3tgw0h3k8gZkG15nSHMQZ1w130_assertion description "[Mutations in the genes for nuclear envelope proteins of emerin (EMD) and lamin A/C (LMNA) are known to cause Emery-Dreifuss muscular dystrophy (EDMD) and limb girdle muscular dystrophy (LGMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145422.RAxOskPvRKMLVKtjE2xHcu3tgw0h3k8gZkG15nSHMQZ1w130_provenance.
- NP145422.RAxOskPvRKMLVKtjE2xHcu3tgw0h3k8gZkG15nSHMQZ1w130_assertion evidence source_evidence_literature NP145422.RAxOskPvRKMLVKtjE2xHcu3tgw0h3k8gZkG15nSHMQZ1w130_provenance.
- NP145422.RAxOskPvRKMLVKtjE2xHcu3tgw0h3k8gZkG15nSHMQZ1w130_assertion SIO_000772 18646565 NP145422.RAxOskPvRKMLVKtjE2xHcu3tgw0h3k8gZkG15nSHMQZ1w130_provenance.
- NP145422.RAxOskPvRKMLVKtjE2xHcu3tgw0h3k8gZkG15nSHMQZ1w130_assertion wasDerivedFrom lhgdn-20090331 NP145422.RAxOskPvRKMLVKtjE2xHcu3tgw0h3k8gZkG15nSHMQZ1w130_provenance.
- NP145422.RAxOskPvRKMLVKtjE2xHcu3tgw0h3k8gZkG15nSHMQZ1w130_assertion wasGeneratedBy ECO_0000203 NP145422.RAxOskPvRKMLVKtjE2xHcu3tgw0h3k8gZkG15nSHMQZ1w130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP145422.RAxOskPvRKMLVKtjE2xHcu3tgw0h3k8gZkG15nSHMQZ1w130_provenance.