Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP425322.RA53rVyT_tmdfxDpDn5g8DCPAAfDS8QguRU2wne662wlw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP425322.RA53rVyT_tmdfxDpDn5g8DCPAAfDS8QguRU2wne662wlw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP425322.RA53rVyT_tmdfxDpDn5g8DCPAAfDS8QguRU2wne662wlw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP425322.RA53rVyT_tmdfxDpDn5g8DCPAAfDS8QguRU2wne662wlw130_provenance.
- NP425322.RA53rVyT_tmdfxDpDn5g8DCPAAfDS8QguRU2wne662wlw130_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." NP425322.RA53rVyT_tmdfxDpDn5g8DCPAAfDS8QguRU2wne662wlw130_provenance.
- NP425322.RA53rVyT_tmdfxDpDn5g8DCPAAfDS8QguRU2wne662wlw130_assertion evidence source_evidence_literature NP425322.RA53rVyT_tmdfxDpDn5g8DCPAAfDS8QguRU2wne662wlw130_provenance.
- NP425322.RA53rVyT_tmdfxDpDn5g8DCPAAfDS8QguRU2wne662wlw130_assertion SIO_000772 14685938 NP425322.RA53rVyT_tmdfxDpDn5g8DCPAAfDS8QguRU2wne662wlw130_provenance.
- NP425322.RA53rVyT_tmdfxDpDn5g8DCPAAfDS8QguRU2wne662wlw130_assertion wasDerivedFrom befree-2016 NP425322.RA53rVyT_tmdfxDpDn5g8DCPAAfDS8QguRU2wne662wlw130_provenance.
- NP425322.RA53rVyT_tmdfxDpDn5g8DCPAAfDS8QguRU2wne662wlw130_assertion wasGeneratedBy ECO_0000203 NP425322.RA53rVyT_tmdfxDpDn5g8DCPAAfDS8QguRU2wne662wlw130_provenance.
- befree-2016 importedOn "2016-02-19" NP425322.RA53rVyT_tmdfxDpDn5g8DCPAAfDS8QguRU2wne662wlw130_provenance.