Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1330494.RAuentUPFJqD1PWhnJ51hPkCqCSWkX08ZmiwmXl996k58130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1330494.RAuentUPFJqD1PWhnJ51hPkCqCSWkX08ZmiwmXl996k58130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1330494.RAuentUPFJqD1PWhnJ51hPkCqCSWkX08ZmiwmXl996k58130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1330494.RAuentUPFJqD1PWhnJ51hPkCqCSWkX08ZmiwmXl996k58130_provenance.
- befree-2016 importedOn "2016-02-19" NP1330494.RAuentUPFJqD1PWhnJ51hPkCqCSWkX08ZmiwmXl996k58130_provenance.
- NP1330494.RAuentUPFJqD1PWhnJ51hPkCqCSWkX08ZmiwmXl996k58130_assertion wasGeneratedBy ECO_0000203 NP1330494.RAuentUPFJqD1PWhnJ51hPkCqCSWkX08ZmiwmXl996k58130_provenance.
- NP1330494.RAuentUPFJqD1PWhnJ51hPkCqCSWkX08ZmiwmXl996k58130_assertion wasDerivedFrom befree-2016 NP1330494.RAuentUPFJqD1PWhnJ51hPkCqCSWkX08ZmiwmXl996k58130_provenance.
- NP1330494.RAuentUPFJqD1PWhnJ51hPkCqCSWkX08ZmiwmXl996k58130_assertion SIO_000772 8037710 NP1330494.RAuentUPFJqD1PWhnJ51hPkCqCSWkX08ZmiwmXl996k58130_provenance.
- NP1330494.RAuentUPFJqD1PWhnJ51hPkCqCSWkX08ZmiwmXl996k58130_assertion evidence source_evidence_literature NP1330494.RAuentUPFJqD1PWhnJ51hPkCqCSWkX08ZmiwmXl996k58130_provenance.
- NP1330494.RAuentUPFJqD1PWhnJ51hPkCqCSWkX08ZmiwmXl996k58130_assertion description "[Genomic analysis by a Polymerase Chain Reaction/Single-Strand Conformation Polymorphism (PCR/SSCP) and direct sequencing indicate the presence of a mutation in exon VII at codon 248 (C to T transition) and a loss of heterozygosity of p53 gene in human rhabdomyosarcoma cell line (RD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1330494.RAuentUPFJqD1PWhnJ51hPkCqCSWkX08ZmiwmXl996k58130_provenance.