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- source_evidence_literature type ECO_0000212 NP105350.RA2O3yUX2p_yyZLuBmL_DQCGg6yAWBuhmoXj1rtcHpxKk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP105350.RA2O3yUX2p_yyZLuBmL_DQCGg6yAWBuhmoXj1rtcHpxKk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP105350.RA2O3yUX2p_yyZLuBmL_DQCGg6yAWBuhmoXj1rtcHpxKk130_provenance.
- NP105350.RA2O3yUX2p_yyZLuBmL_DQCGg6yAWBuhmoXj1rtcHpxKk130_assertion description "[there was no significant difference in frequency of p53 mutation among patients with different genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP105350.RA2O3yUX2p_yyZLuBmL_DQCGg6yAWBuhmoXj1rtcHpxKk130_provenance.
- NP105350.RA2O3yUX2p_yyZLuBmL_DQCGg6yAWBuhmoXj1rtcHpxKk130_assertion evidence source_evidence_literature NP105350.RA2O3yUX2p_yyZLuBmL_DQCGg6yAWBuhmoXj1rtcHpxKk130_provenance.
- NP105350.RA2O3yUX2p_yyZLuBmL_DQCGg6yAWBuhmoXj1rtcHpxKk130_assertion SIO_000772 15499621 NP105350.RA2O3yUX2p_yyZLuBmL_DQCGg6yAWBuhmoXj1rtcHpxKk130_provenance.
- NP105350.RA2O3yUX2p_yyZLuBmL_DQCGg6yAWBuhmoXj1rtcHpxKk130_assertion wasDerivedFrom gad-20150221 NP105350.RA2O3yUX2p_yyZLuBmL_DQCGg6yAWBuhmoXj1rtcHpxKk130_provenance.
- NP105350.RA2O3yUX2p_yyZLuBmL_DQCGg6yAWBuhmoXj1rtcHpxKk130_assertion wasGeneratedBy ECO_0000203 NP105350.RA2O3yUX2p_yyZLuBmL_DQCGg6yAWBuhmoXj1rtcHpxKk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP105350.RA2O3yUX2p_yyZLuBmL_DQCGg6yAWBuhmoXj1rtcHpxKk130_provenance.