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- source_evidence_literature type ECO_0000212 NP509723.RAwEK6l7Ox7l1Y-oIsJ-PYw_dXWg4Dq68BfM3F9xAyk3c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP509723.RAwEK6l7Ox7l1Y-oIsJ-PYw_dXWg4Dq68BfM3F9xAyk3c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP509723.RAwEK6l7Ox7l1Y-oIsJ-PYw_dXWg4Dq68BfM3F9xAyk3c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP509723.RAwEK6l7Ox7l1Y-oIsJ-PYw_dXWg4Dq68BfM3F9xAyk3c130_provenance.
- NP509723.RAwEK6l7Ox7l1Y-oIsJ-PYw_dXWg4Dq68BfM3F9xAyk3c130_assertion wasGeneratedBy ECO_0000203 NP509723.RAwEK6l7Ox7l1Y-oIsJ-PYw_dXWg4Dq68BfM3F9xAyk3c130_provenance.
- NP509723.RAwEK6l7Ox7l1Y-oIsJ-PYw_dXWg4Dq68BfM3F9xAyk3c130_assertion wasDerivedFrom befree-20150227 NP509723.RAwEK6l7Ox7l1Y-oIsJ-PYw_dXWg4Dq68BfM3F9xAyk3c130_provenance.
- NP509723.RAwEK6l7Ox7l1Y-oIsJ-PYw_dXWg4Dq68BfM3F9xAyk3c130_assertion SIO_000772 14676120 NP509723.RAwEK6l7Ox7l1Y-oIsJ-PYw_dXWg4Dq68BfM3F9xAyk3c130_provenance.
- NP509723.RAwEK6l7Ox7l1Y-oIsJ-PYw_dXWg4Dq68BfM3F9xAyk3c130_assertion evidence source_evidence_literature NP509723.RAwEK6l7Ox7l1Y-oIsJ-PYw_dXWg4Dq68BfM3F9xAyk3c130_provenance.
- NP509723.RAwEK6l7Ox7l1Y-oIsJ-PYw_dXWg4Dq68BfM3F9xAyk3c130_assertion description "[Our data indicate that although mutations of ING1 seem to be infrequent in human brain tumors, deregulated expression and mislocalization of ING1 proteins, particularly the p33ING1b isoform, are common events in gliomas and glioblastomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP509723.RAwEK6l7Ox7l1Y-oIsJ-PYw_dXWg4Dq68BfM3F9xAyk3c130_provenance.