Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP473940.RAxz9Rp59qrb8ZV2fhDHBLEGVVcLMtyVECxGxFwNcgIDM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP473940.RAxz9Rp59qrb8ZV2fhDHBLEGVVcLMtyVECxGxFwNcgIDM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP473940.RAxz9Rp59qrb8ZV2fhDHBLEGVVcLMtyVECxGxFwNcgIDM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP473940.RAxz9Rp59qrb8ZV2fhDHBLEGVVcLMtyVECxGxFwNcgIDM130_provenance.
- NP473940.RAxz9Rp59qrb8ZV2fhDHBLEGVVcLMtyVECxGxFwNcgIDM130_assertion description "[Limb-girdle muscular dystrophy type 1D (LGMD1D) was linked to chromosome 7q36 over a decade ago, but its genetic cause has remained elusive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP473940.RAxz9Rp59qrb8ZV2fhDHBLEGVVcLMtyVECxGxFwNcgIDM130_provenance.
- NP473940.RAxz9Rp59qrb8ZV2fhDHBLEGVVcLMtyVECxGxFwNcgIDM130_assertion evidence source_evidence_literature NP473940.RAxz9Rp59qrb8ZV2fhDHBLEGVVcLMtyVECxGxFwNcgIDM130_provenance.
- NP473940.RAxz9Rp59qrb8ZV2fhDHBLEGVVcLMtyVECxGxFwNcgIDM130_assertion SIO_000772 22366786 NP473940.RAxz9Rp59qrb8ZV2fhDHBLEGVVcLMtyVECxGxFwNcgIDM130_provenance.
- NP473940.RAxz9Rp59qrb8ZV2fhDHBLEGVVcLMtyVECxGxFwNcgIDM130_assertion wasDerivedFrom befree-20140225 NP473940.RAxz9Rp59qrb8ZV2fhDHBLEGVVcLMtyVECxGxFwNcgIDM130_provenance.
- NP473940.RAxz9Rp59qrb8ZV2fhDHBLEGVVcLMtyVECxGxFwNcgIDM130_assertion wasGeneratedBy ECO_0000203 NP473940.RAxz9Rp59qrb8ZV2fhDHBLEGVVcLMtyVECxGxFwNcgIDM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP473940.RAxz9Rp59qrb8ZV2fhDHBLEGVVcLMtyVECxGxFwNcgIDM130_provenance.