Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP812172.RADtZXcpanvF8PDAIqiyPwSOGFC6rrOpidrrwj9vxR1vA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP812172.RADtZXcpanvF8PDAIqiyPwSOGFC6rrOpidrrwj9vxR1vA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP812172.RADtZXcpanvF8PDAIqiyPwSOGFC6rrOpidrrwj9vxR1vA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP812172.RADtZXcpanvF8PDAIqiyPwSOGFC6rrOpidrrwj9vxR1vA130_provenance.
- NP812172.RADtZXcpanvF8PDAIqiyPwSOGFC6rrOpidrrwj9vxR1vA130_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." NP812172.RADtZXcpanvF8PDAIqiyPwSOGFC6rrOpidrrwj9vxR1vA130_provenance.
- NP812172.RADtZXcpanvF8PDAIqiyPwSOGFC6rrOpidrrwj9vxR1vA130_assertion evidence source_evidence_literature NP812172.RADtZXcpanvF8PDAIqiyPwSOGFC6rrOpidrrwj9vxR1vA130_provenance.
- NP812172.RADtZXcpanvF8PDAIqiyPwSOGFC6rrOpidrrwj9vxR1vA130_assertion SIO_000772 18646565 NP812172.RADtZXcpanvF8PDAIqiyPwSOGFC6rrOpidrrwj9vxR1vA130_provenance.
- NP812172.RADtZXcpanvF8PDAIqiyPwSOGFC6rrOpidrrwj9vxR1vA130_assertion wasDerivedFrom befree-20140225 NP812172.RADtZXcpanvF8PDAIqiyPwSOGFC6rrOpidrrwj9vxR1vA130_provenance.
- NP812172.RADtZXcpanvF8PDAIqiyPwSOGFC6rrOpidrrwj9vxR1vA130_assertion wasGeneratedBy ECO_0000203 NP812172.RADtZXcpanvF8PDAIqiyPwSOGFC6rrOpidrrwj9vxR1vA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP812172.RADtZXcpanvF8PDAIqiyPwSOGFC6rrOpidrrwj9vxR1vA130_provenance.