Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_provenance.
- NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_assertion description "[The SSCP technique showed heterozygous defects in the p53 gene in 8 of 39 (20.5%) melanoma tumors: three point mutations in intron sequences (introns 1 and 2) and exon 10, and three new polymorphisms located in introns 1 and 2 (C to T transition at position 11701 in intron 1; C insertion at position 11818 in intron 2; and C insertion at position 11875 in intron 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_provenance.
- NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_assertion evidence source_evidence_literature NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_provenance.
- NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_assertion SIO_000772 15960923 NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_provenance.
- NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_assertion wasDerivedFrom befree-2016 NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_provenance.
- NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_assertion wasGeneratedBy ECO_0000203 NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_provenance.
- befree-2016 importedOn "2016-02-19" NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_provenance.