Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP917936.RAb17TFt9MwJUdT58581hXMeQMTe1xcX5DDT1zWXb_8OE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP917936.RAb17TFt9MwJUdT58581hXMeQMTe1xcX5DDT1zWXb_8OE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP917936.RAb17TFt9MwJUdT58581hXMeQMTe1xcX5DDT1zWXb_8OE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP917936.RAb17TFt9MwJUdT58581hXMeQMTe1xcX5DDT1zWXb_8OE130_provenance.
- NP917936.RAb17TFt9MwJUdT58581hXMeQMTe1xcX5DDT1zWXb_8OE130_assertion description "[Our results demonstrated that some copy number changes thought to belong to early (MDM4 gain) or late stage (MYCN and E2F3 gain) of retinoblastoma are already present in retinoma at the same (for MDM4) or at lower (for MYCN and E2F3) copy number variation respect to retinoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917936.RAb17TFt9MwJUdT58581hXMeQMTe1xcX5DDT1zWXb_8OE130_provenance.
- NP917936.RAb17TFt9MwJUdT58581hXMeQMTe1xcX5DDT1zWXb_8OE130_assertion evidence source_evidence_literature NP917936.RAb17TFt9MwJUdT58581hXMeQMTe1xcX5DDT1zWXb_8OE130_provenance.
- NP917936.RAb17TFt9MwJUdT58581hXMeQMTe1xcX5DDT1zWXb_8OE130_assertion SIO_000772 18785023 NP917936.RAb17TFt9MwJUdT58581hXMeQMTe1xcX5DDT1zWXb_8OE130_provenance.
- NP917936.RAb17TFt9MwJUdT58581hXMeQMTe1xcX5DDT1zWXb_8OE130_assertion wasDerivedFrom befree-20140225 NP917936.RAb17TFt9MwJUdT58581hXMeQMTe1xcX5DDT1zWXb_8OE130_provenance.
- NP917936.RAb17TFt9MwJUdT58581hXMeQMTe1xcX5DDT1zWXb_8OE130_assertion wasGeneratedBy ECO_0000203 NP917936.RAb17TFt9MwJUdT58581hXMeQMTe1xcX5DDT1zWXb_8OE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP917936.RAb17TFt9MwJUdT58581hXMeQMTe1xcX5DDT1zWXb_8OE130_provenance.