Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP205253.RA_ZzdebHFxnLGhDbdN1VsemynD4Y22y3u6n1V-OfOYtg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP205253.RA_ZzdebHFxnLGhDbdN1VsemynD4Y22y3u6n1V-OfOYtg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP205253.RA_ZzdebHFxnLGhDbdN1VsemynD4Y22y3u6n1V-OfOYtg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP205253.RA_ZzdebHFxnLGhDbdN1VsemynD4Y22y3u6n1V-OfOYtg130_provenance.
- NP205253.RA_ZzdebHFxnLGhDbdN1VsemynD4Y22y3u6n1V-OfOYtg130_assertion description "[Emery-Dreifuss muscular dystrophy (EDMD1) is caused by mutations in either the X-linked gene emerin (EMD) or the autosomal lamin A/C (LMNA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205253.RA_ZzdebHFxnLGhDbdN1VsemynD4Y22y3u6n1V-OfOYtg130_provenance.
- NP205253.RA_ZzdebHFxnLGhDbdN1VsemynD4Y22y3u6n1V-OfOYtg130_assertion evidence source_evidence_literature NP205253.RA_ZzdebHFxnLGhDbdN1VsemynD4Y22y3u6n1V-OfOYtg130_provenance.
- NP205253.RA_ZzdebHFxnLGhDbdN1VsemynD4Y22y3u6n1V-OfOYtg130_assertion SIO_000772 16403804 NP205253.RA_ZzdebHFxnLGhDbdN1VsemynD4Y22y3u6n1V-OfOYtg130_provenance.
- NP205253.RA_ZzdebHFxnLGhDbdN1VsemynD4Y22y3u6n1V-OfOYtg130_assertion wasDerivedFrom befree-20140225 NP205253.RA_ZzdebHFxnLGhDbdN1VsemynD4Y22y3u6n1V-OfOYtg130_provenance.
- NP205253.RA_ZzdebHFxnLGhDbdN1VsemynD4Y22y3u6n1V-OfOYtg130_assertion wasGeneratedBy ECO_0000203 NP205253.RA_ZzdebHFxnLGhDbdN1VsemynD4Y22y3u6n1V-OfOYtg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP205253.RA_ZzdebHFxnLGhDbdN1VsemynD4Y22y3u6n1V-OfOYtg130_provenance.