Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP150387.RAfghd4yBTX7znpYa3aYCf99qoktuCRtZvEUtcaGNCgho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP150387.RAfghd4yBTX7znpYa3aYCf99qoktuCRtZvEUtcaGNCgho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP150387.RAfghd4yBTX7znpYa3aYCf99qoktuCRtZvEUtcaGNCgho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP150387.RAfghd4yBTX7znpYa3aYCf99qoktuCRtZvEUtcaGNCgho130_provenance.
- NP150387.RAfghd4yBTX7znpYa3aYCf99qoktuCRtZvEUtcaGNCgho130_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." NP150387.RAfghd4yBTX7znpYa3aYCf99qoktuCRtZvEUtcaGNCgho130_provenance.
- NP150387.RAfghd4yBTX7znpYa3aYCf99qoktuCRtZvEUtcaGNCgho130_assertion evidence source_evidence_literature NP150387.RAfghd4yBTX7znpYa3aYCf99qoktuCRtZvEUtcaGNCgho130_provenance.
- NP150387.RAfghd4yBTX7znpYa3aYCf99qoktuCRtZvEUtcaGNCgho130_assertion SIO_000772 18646565 NP150387.RAfghd4yBTX7znpYa3aYCf99qoktuCRtZvEUtcaGNCgho130_provenance.
- NP150387.RAfghd4yBTX7znpYa3aYCf99qoktuCRtZvEUtcaGNCgho130_assertion wasDerivedFrom lhgdn-20090331 NP150387.RAfghd4yBTX7znpYa3aYCf99qoktuCRtZvEUtcaGNCgho130_provenance.
- NP150387.RAfghd4yBTX7znpYa3aYCf99qoktuCRtZvEUtcaGNCgho130_assertion wasGeneratedBy ECO_0000203 NP150387.RAfghd4yBTX7znpYa3aYCf99qoktuCRtZvEUtcaGNCgho130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP150387.RAfghd4yBTX7znpYa3aYCf99qoktuCRtZvEUtcaGNCgho130_provenance.