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- source_evidence_literature type ECO_0000212 NP795642.RAhtKW3JUutKwA0Q2700oc3bMM-eCqzoo_Em6ALpTOWfI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795642.RAhtKW3JUutKwA0Q2700oc3bMM-eCqzoo_Em6ALpTOWfI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795642.RAhtKW3JUutKwA0Q2700oc3bMM-eCqzoo_Em6ALpTOWfI130_provenance.
- NP795642.RAhtKW3JUutKwA0Q2700oc3bMM-eCqzoo_Em6ALpTOWfI130_assertion description "[Overall frequency of SPOP mutations was 8.1% (4.6% to 14.4%), SPOP mutation was inversely associated with ERG rearrangement (P<.01), and SPOP mutant (SPOPmut) cancers had higher rates of CHD1 deletions (P<.01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795642.RAhtKW3JUutKwA0Q2700oc3bMM-eCqzoo_Em6ALpTOWfI130_provenance.
- NP795642.RAhtKW3JUutKwA0Q2700oc3bMM-eCqzoo_Em6ALpTOWfI130_assertion evidence source_evidence_literature NP795642.RAhtKW3JUutKwA0Q2700oc3bMM-eCqzoo_Em6ALpTOWfI130_provenance.
- NP795642.RAhtKW3JUutKwA0Q2700oc3bMM-eCqzoo_Em6ALpTOWfI130_assertion SIO_000772 24563616 NP795642.RAhtKW3JUutKwA0Q2700oc3bMM-eCqzoo_Em6ALpTOWfI130_provenance.
- NP795642.RAhtKW3JUutKwA0Q2700oc3bMM-eCqzoo_Em6ALpTOWfI130_assertion wasDerivedFrom befree-20150227 NP795642.RAhtKW3JUutKwA0Q2700oc3bMM-eCqzoo_Em6ALpTOWfI130_provenance.
- NP795642.RAhtKW3JUutKwA0Q2700oc3bMM-eCqzoo_Em6ALpTOWfI130_assertion wasGeneratedBy ECO_0000203 NP795642.RAhtKW3JUutKwA0Q2700oc3bMM-eCqzoo_Em6ALpTOWfI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP795642.RAhtKW3JUutKwA0Q2700oc3bMM-eCqzoo_Em6ALpTOWfI130_provenance.