Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1371152.RAEYpqV9T5MmxACB79ptEmuSQMHd3BQl42Bam5N9_pgfw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1371152.RAEYpqV9T5MmxACB79ptEmuSQMHd3BQl42Bam5N9_pgfw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1371152.RAEYpqV9T5MmxACB79ptEmuSQMHd3BQl42Bam5N9_pgfw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1371152.RAEYpqV9T5MmxACB79ptEmuSQMHd3BQl42Bam5N9_pgfw130_provenance.
- NP1371152.RAEYpqV9T5MmxACB79ptEmuSQMHd3BQl42Bam5N9_pgfw130_assertion description "[We analyzed 26 neuroblastomas, two ganglioneuromas, and a neuroblastoma metastasis for mutations and homozygous deletions of the p16 (or MTS1 or CDKN2) gene by means of the polymerase chain reaction (PCR) in combination with the single-strand conformation polymorphism (SSCP) technique and by multiplex PCR analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1371152.RAEYpqV9T5MmxACB79ptEmuSQMHd3BQl42Bam5N9_pgfw130_provenance.
- NP1371152.RAEYpqV9T5MmxACB79ptEmuSQMHd3BQl42Bam5N9_pgfw130_assertion evidence source_evidence_literature NP1371152.RAEYpqV9T5MmxACB79ptEmuSQMHd3BQl42Bam5N9_pgfw130_provenance.
- NP1371152.RAEYpqV9T5MmxACB79ptEmuSQMHd3BQl42Bam5N9_pgfw130_assertion SIO_000772 9115582 NP1371152.RAEYpqV9T5MmxACB79ptEmuSQMHd3BQl42Bam5N9_pgfw130_provenance.
- NP1371152.RAEYpqV9T5MmxACB79ptEmuSQMHd3BQl42Bam5N9_pgfw130_assertion wasDerivedFrom befree-2016 NP1371152.RAEYpqV9T5MmxACB79ptEmuSQMHd3BQl42Bam5N9_pgfw130_provenance.
- NP1371152.RAEYpqV9T5MmxACB79ptEmuSQMHd3BQl42Bam5N9_pgfw130_assertion wasGeneratedBy ECO_0000203 NP1371152.RAEYpqV9T5MmxACB79ptEmuSQMHd3BQl42Bam5N9_pgfw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1371152.RAEYpqV9T5MmxACB79ptEmuSQMHd3BQl42Bam5N9_pgfw130_provenance.