Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP688747.RAWNuKtgAoMfrFKPwHpFyViB3adBTYwfSqlPuid11iE4E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP688747.RAWNuKtgAoMfrFKPwHpFyViB3adBTYwfSqlPuid11iE4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP688747.RAWNuKtgAoMfrFKPwHpFyViB3adBTYwfSqlPuid11iE4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP688747.RAWNuKtgAoMfrFKPwHpFyViB3adBTYwfSqlPuid11iE4E130_provenance.
- NP688747.RAWNuKtgAoMfrFKPwHpFyViB3adBTYwfSqlPuid11iE4E130_assertion description "[A registry of early-onset RCCs revealed a family comprising a son with clear-cell RCC and his mother with a cardiac tumor, both with the germline SDHB R27X mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP688747.RAWNuKtgAoMfrFKPwHpFyViB3adBTYwfSqlPuid11iE4E130_provenance.
- NP688747.RAWNuKtgAoMfrFKPwHpFyViB3adBTYwfSqlPuid11iE4E130_assertion evidence source_evidence_literature NP688747.RAWNuKtgAoMfrFKPwHpFyViB3adBTYwfSqlPuid11iE4E130_provenance.
- NP688747.RAWNuKtgAoMfrFKPwHpFyViB3adBTYwfSqlPuid11iE4E130_assertion SIO_000772 14685938 NP688747.RAWNuKtgAoMfrFKPwHpFyViB3adBTYwfSqlPuid11iE4E130_provenance.
- NP688747.RAWNuKtgAoMfrFKPwHpFyViB3adBTYwfSqlPuid11iE4E130_assertion wasDerivedFrom befree-20150227 NP688747.RAWNuKtgAoMfrFKPwHpFyViB3adBTYwfSqlPuid11iE4E130_provenance.
- NP688747.RAWNuKtgAoMfrFKPwHpFyViB3adBTYwfSqlPuid11iE4E130_assertion wasGeneratedBy ECO_0000203 NP688747.RAWNuKtgAoMfrFKPwHpFyViB3adBTYwfSqlPuid11iE4E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP688747.RAWNuKtgAoMfrFKPwHpFyViB3adBTYwfSqlPuid11iE4E130_provenance.