Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP478350.RAUeL4I-qUKD0FLN54ZmXYtTeQ7nqowuQyypMqqCf-nf8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP478350.RAUeL4I-qUKD0FLN54ZmXYtTeQ7nqowuQyypMqqCf-nf8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478350.RAUeL4I-qUKD0FLN54ZmXYtTeQ7nqowuQyypMqqCf-nf8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478350.RAUeL4I-qUKD0FLN54ZmXYtTeQ7nqowuQyypMqqCf-nf8130_provenance.
- NP478350.RAUeL4I-qUKD0FLN54ZmXYtTeQ7nqowuQyypMqqCf-nf8130_assertion description "[To define the location and extent of deletions of 9p in NSCLC and MM, Southern blot analyses on six NSCLC and five MM cell lines using molecular probes to 9p loci (IFNA, IFNB1, D9S3, and D9S19) were performed, and DNA dosage was determined by densitometry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478350.RAUeL4I-qUKD0FLN54ZmXYtTeQ7nqowuQyypMqqCf-nf8130_provenance.
- NP478350.RAUeL4I-qUKD0FLN54ZmXYtTeQ7nqowuQyypMqqCf-nf8130_assertion evidence source_evidence_literature NP478350.RAUeL4I-qUKD0FLN54ZmXYtTeQ7nqowuQyypMqqCf-nf8130_provenance.
- NP478350.RAUeL4I-qUKD0FLN54ZmXYtTeQ7nqowuQyypMqqCf-nf8130_assertion SIO_000772 7688555 NP478350.RAUeL4I-qUKD0FLN54ZmXYtTeQ7nqowuQyypMqqCf-nf8130_provenance.
- NP478350.RAUeL4I-qUKD0FLN54ZmXYtTeQ7nqowuQyypMqqCf-nf8130_assertion wasDerivedFrom befree-20150227 NP478350.RAUeL4I-qUKD0FLN54ZmXYtTeQ7nqowuQyypMqqCf-nf8130_provenance.
- NP478350.RAUeL4I-qUKD0FLN54ZmXYtTeQ7nqowuQyypMqqCf-nf8130_assertion wasGeneratedBy ECO_0000203 NP478350.RAUeL4I-qUKD0FLN54ZmXYtTeQ7nqowuQyypMqqCf-nf8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP478350.RAUeL4I-qUKD0FLN54ZmXYtTeQ7nqowuQyypMqqCf-nf8130_provenance.