Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP925775.RA5BhHfi08X7zFXyRrb3VhXFq9Nbh596GhX1uWl6W6fP0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925775.RA5BhHfi08X7zFXyRrb3VhXFq9Nbh596GhX1uWl6W6fP0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925775.RA5BhHfi08X7zFXyRrb3VhXFq9Nbh596GhX1uWl6W6fP0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925775.RA5BhHfi08X7zFXyRrb3VhXFq9Nbh596GhX1uWl6W6fP0130_provenance.
- NP925775.RA5BhHfi08X7zFXyRrb3VhXFq9Nbh596GhX1uWl6W6fP0130_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." NP925775.RA5BhHfi08X7zFXyRrb3VhXFq9Nbh596GhX1uWl6W6fP0130_provenance.
- NP925775.RA5BhHfi08X7zFXyRrb3VhXFq9Nbh596GhX1uWl6W6fP0130_assertion evidence source_evidence_literature NP925775.RA5BhHfi08X7zFXyRrb3VhXFq9Nbh596GhX1uWl6W6fP0130_provenance.
- NP925775.RA5BhHfi08X7zFXyRrb3VhXFq9Nbh596GhX1uWl6W6fP0130_assertion SIO_000772 9115582 NP925775.RA5BhHfi08X7zFXyRrb3VhXFq9Nbh596GhX1uWl6W6fP0130_provenance.
- NP925775.RA5BhHfi08X7zFXyRrb3VhXFq9Nbh596GhX1uWl6W6fP0130_assertion wasDerivedFrom befree-20140225 NP925775.RA5BhHfi08X7zFXyRrb3VhXFq9Nbh596GhX1uWl6W6fP0130_provenance.
- NP925775.RA5BhHfi08X7zFXyRrb3VhXFq9Nbh596GhX1uWl6W6fP0130_assertion wasGeneratedBy ECO_0000203 NP925775.RA5BhHfi08X7zFXyRrb3VhXFq9Nbh596GhX1uWl6W6fP0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP925775.RA5BhHfi08X7zFXyRrb3VhXFq9Nbh596GhX1uWl6W6fP0130_provenance.