Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP889199.RAtL9T6yaGwpnGXmrPgyf5FZqFkQ5Q0PwRISthpXT4j6E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP889199.RAtL9T6yaGwpnGXmrPgyf5FZqFkQ5Q0PwRISthpXT4j6E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889199.RAtL9T6yaGwpnGXmrPgyf5FZqFkQ5Q0PwRISthpXT4j6E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889199.RAtL9T6yaGwpnGXmrPgyf5FZqFkQ5Q0PwRISthpXT4j6E130_provenance.
- NP889199.RAtL9T6yaGwpnGXmrPgyf5FZqFkQ5Q0PwRISthpXT4j6E130_assertion description "[Since it has been proposed that especially neoplasias lacking p53 alterations might show a loss of heterozygosity at 1p35-1p36, we studied the frequency of p53 and p73 deletions in bone marrow mononuclear cells of 68 patients with MM, two patients with monoclonal gammopathy of undetermined significance and four patients with plasma cell leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889199.RAtL9T6yaGwpnGXmrPgyf5FZqFkQ5Q0PwRISthpXT4j6E130_provenance.
- NP889199.RAtL9T6yaGwpnGXmrPgyf5FZqFkQ5Q0PwRISthpXT4j6E130_assertion evidence source_evidence_literature NP889199.RAtL9T6yaGwpnGXmrPgyf5FZqFkQ5Q0PwRISthpXT4j6E130_provenance.
- NP889199.RAtL9T6yaGwpnGXmrPgyf5FZqFkQ5Q0PwRISthpXT4j6E130_assertion SIO_000772 10602435 NP889199.RAtL9T6yaGwpnGXmrPgyf5FZqFkQ5Q0PwRISthpXT4j6E130_provenance.
- NP889199.RAtL9T6yaGwpnGXmrPgyf5FZqFkQ5Q0PwRISthpXT4j6E130_assertion wasDerivedFrom befree-20140225 NP889199.RAtL9T6yaGwpnGXmrPgyf5FZqFkQ5Q0PwRISthpXT4j6E130_provenance.
- NP889199.RAtL9T6yaGwpnGXmrPgyf5FZqFkQ5Q0PwRISthpXT4j6E130_assertion wasGeneratedBy ECO_0000203 NP889199.RAtL9T6yaGwpnGXmrPgyf5FZqFkQ5Q0PwRISthpXT4j6E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP889199.RAtL9T6yaGwpnGXmrPgyf5FZqFkQ5Q0PwRISthpXT4j6E130_provenance.