Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP930513.RAYjAJbbRw4QGEp1Ue8oHUZc0nDpibB78_OBljs-LUXWM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP930513.RAYjAJbbRw4QGEp1Ue8oHUZc0nDpibB78_OBljs-LUXWM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP930513.RAYjAJbbRw4QGEp1Ue8oHUZc0nDpibB78_OBljs-LUXWM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP930513.RAYjAJbbRw4QGEp1Ue8oHUZc0nDpibB78_OBljs-LUXWM130_provenance.
- NP930513.RAYjAJbbRw4QGEp1Ue8oHUZc0nDpibB78_OBljs-LUXWM130_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." NP930513.RAYjAJbbRw4QGEp1Ue8oHUZc0nDpibB78_OBljs-LUXWM130_provenance.
- NP930513.RAYjAJbbRw4QGEp1Ue8oHUZc0nDpibB78_OBljs-LUXWM130_assertion evidence source_evidence_literature NP930513.RAYjAJbbRw4QGEp1Ue8oHUZc0nDpibB78_OBljs-LUXWM130_provenance.
- NP930513.RAYjAJbbRw4QGEp1Ue8oHUZc0nDpibB78_OBljs-LUXWM130_assertion SIO_000772 14685938 NP930513.RAYjAJbbRw4QGEp1Ue8oHUZc0nDpibB78_OBljs-LUXWM130_provenance.
- NP930513.RAYjAJbbRw4QGEp1Ue8oHUZc0nDpibB78_OBljs-LUXWM130_assertion wasDerivedFrom befree-20140225 NP930513.RAYjAJbbRw4QGEp1Ue8oHUZc0nDpibB78_OBljs-LUXWM130_provenance.
- NP930513.RAYjAJbbRw4QGEp1Ue8oHUZc0nDpibB78_OBljs-LUXWM130_assertion wasGeneratedBy ECO_0000203 NP930513.RAYjAJbbRw4QGEp1Ue8oHUZc0nDpibB78_OBljs-LUXWM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP930513.RAYjAJbbRw4QGEp1Ue8oHUZc0nDpibB78_OBljs-LUXWM130_provenance.