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- source_evidence_literature type ECO_0000212 NP373872.RASs97jS6FOWDYqrG06QjNy_7lSf9cgZnbev4G0wqJ1JI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP373872.RASs97jS6FOWDYqrG06QjNy_7lSf9cgZnbev4G0wqJ1JI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP373872.RASs97jS6FOWDYqrG06QjNy_7lSf9cgZnbev4G0wqJ1JI130_provenance.
- NP373872.RASs97jS6FOWDYqrG06QjNy_7lSf9cgZnbev4G0wqJ1JI130_assertion description "[This showed that the two nuclear envelope defects (EDMD LMNA, EDMD emerin) were highly related disorders and were also related to fascioscapulohumeral muscular dystrophy (FSHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP373872.RASs97jS6FOWDYqrG06QjNy_7lSf9cgZnbev4G0wqJ1JI130_provenance.
- NP373872.RASs97jS6FOWDYqrG06QjNy_7lSf9cgZnbev4G0wqJ1JI130_assertion evidence source_evidence_literature NP373872.RASs97jS6FOWDYqrG06QjNy_7lSf9cgZnbev4G0wqJ1JI130_provenance.
- NP373872.RASs97jS6FOWDYqrG06QjNy_7lSf9cgZnbev4G0wqJ1JI130_assertion SIO_000772 16478798 NP373872.RASs97jS6FOWDYqrG06QjNy_7lSf9cgZnbev4G0wqJ1JI130_provenance.
- NP373872.RASs97jS6FOWDYqrG06QjNy_7lSf9cgZnbev4G0wqJ1JI130_assertion wasDerivedFrom befree-20150227 NP373872.RASs97jS6FOWDYqrG06QjNy_7lSf9cgZnbev4G0wqJ1JI130_provenance.
- NP373872.RASs97jS6FOWDYqrG06QjNy_7lSf9cgZnbev4G0wqJ1JI130_assertion wasGeneratedBy ECO_0000203 NP373872.RASs97jS6FOWDYqrG06QjNy_7lSf9cgZnbev4G0wqJ1JI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP373872.RASs97jS6FOWDYqrG06QjNy_7lSf9cgZnbev4G0wqJ1JI130_provenance.