Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP453010.RA20SB-UN6TN_BnAba6RDzgUx1kZPTsEf5wvZ93vRHGic130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP453010.RA20SB-UN6TN_BnAba6RDzgUx1kZPTsEf5wvZ93vRHGic130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP453010.RA20SB-UN6TN_BnAba6RDzgUx1kZPTsEf5wvZ93vRHGic130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP453010.RA20SB-UN6TN_BnAba6RDzgUx1kZPTsEf5wvZ93vRHGic130_provenance.
- NP453010.RA20SB-UN6TN_BnAba6RDzgUx1kZPTsEf5wvZ93vRHGic130_assertion description "[We have reported frequent allele loss for the marker HRAS on chromosome 11p in human lung cancer and defined the smallest common region of deletion (designated LOH11B) to approximately 500 kb.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453010.RA20SB-UN6TN_BnAba6RDzgUx1kZPTsEf5wvZ93vRHGic130_provenance.
- NP453010.RA20SB-UN6TN_BnAba6RDzgUx1kZPTsEf5wvZ93vRHGic130_assertion evidence source_evidence_literature NP453010.RA20SB-UN6TN_BnAba6RDzgUx1kZPTsEf5wvZ93vRHGic130_provenance.
- NP453010.RA20SB-UN6TN_BnAba6RDzgUx1kZPTsEf5wvZ93vRHGic130_assertion SIO_000772 9149890 NP453010.RA20SB-UN6TN_BnAba6RDzgUx1kZPTsEf5wvZ93vRHGic130_provenance.
- NP453010.RA20SB-UN6TN_BnAba6RDzgUx1kZPTsEf5wvZ93vRHGic130_assertion wasDerivedFrom befree-20140225 NP453010.RA20SB-UN6TN_BnAba6RDzgUx1kZPTsEf5wvZ93vRHGic130_provenance.
- NP453010.RA20SB-UN6TN_BnAba6RDzgUx1kZPTsEf5wvZ93vRHGic130_assertion wasGeneratedBy ECO_0000203 NP453010.RA20SB-UN6TN_BnAba6RDzgUx1kZPTsEf5wvZ93vRHGic130_provenance.
- befree-20140225 importedOn "2014-02-25" NP453010.RA20SB-UN6TN_BnAba6RDzgUx1kZPTsEf5wvZ93vRHGic130_provenance.