Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP689163.RA-ADpleF9r0qq9P_TpLvBdXc7wlaHLMUPmXeo-YmzFcU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP689163.RA-ADpleF9r0qq9P_TpLvBdXc7wlaHLMUPmXeo-YmzFcU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP689163.RA-ADpleF9r0qq9P_TpLvBdXc7wlaHLMUPmXeo-YmzFcU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP689163.RA-ADpleF9r0qq9P_TpLvBdXc7wlaHLMUPmXeo-YmzFcU130_provenance.
- NP689163.RA-ADpleF9r0qq9P_TpLvBdXc7wlaHLMUPmXeo-YmzFcU130_assertion description "[Mutation detection rates were highest in those with a positive family history (62%), malignancy (53%), multiple tumours (33%) or PGL (44%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689163.RA-ADpleF9r0qq9P_TpLvBdXc7wlaHLMUPmXeo-YmzFcU130_provenance.
- NP689163.RA-ADpleF9r0qq9P_TpLvBdXc7wlaHLMUPmXeo-YmzFcU130_assertion evidence source_evidence_literature NP689163.RA-ADpleF9r0qq9P_TpLvBdXc7wlaHLMUPmXeo-YmzFcU130_provenance.
- NP689163.RA-ADpleF9r0qq9P_TpLvBdXc7wlaHLMUPmXeo-YmzFcU130_assertion SIO_000772 23072324 NP689163.RA-ADpleF9r0qq9P_TpLvBdXc7wlaHLMUPmXeo-YmzFcU130_provenance.
- NP689163.RA-ADpleF9r0qq9P_TpLvBdXc7wlaHLMUPmXeo-YmzFcU130_assertion wasDerivedFrom befree-20150227 NP689163.RA-ADpleF9r0qq9P_TpLvBdXc7wlaHLMUPmXeo-YmzFcU130_provenance.
- NP689163.RA-ADpleF9r0qq9P_TpLvBdXc7wlaHLMUPmXeo-YmzFcU130_assertion wasGeneratedBy ECO_0000203 NP689163.RA-ADpleF9r0qq9P_TpLvBdXc7wlaHLMUPmXeo-YmzFcU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP689163.RA-ADpleF9r0qq9P_TpLvBdXc7wlaHLMUPmXeo-YmzFcU130_provenance.