Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP470790.RAT1UaChLCqVsUemFg55aRK7cPg1N-gKfP4svz4P_FFPQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP470790.RAT1UaChLCqVsUemFg55aRK7cPg1N-gKfP4svz4P_FFPQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470790.RAT1UaChLCqVsUemFg55aRK7cPg1N-gKfP4svz4P_FFPQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470790.RAT1UaChLCqVsUemFg55aRK7cPg1N-gKfP4svz4P_FFPQ130_provenance.
- NP470790.RAT1UaChLCqVsUemFg55aRK7cPg1N-gKfP4svz4P_FFPQ130_assertion description "[Although hst gene rearrangements and deletions of 11q13 are not associated with sporadic PRL-cell adenoma formation, a single patient was detected with a partial loss of chromosome 11, including the putative MEN-1 site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470790.RAT1UaChLCqVsUemFg55aRK7cPg1N-gKfP4svz4P_FFPQ130_provenance.
- NP470790.RAT1UaChLCqVsUemFg55aRK7cPg1N-gKfP4svz4P_FFPQ130_assertion evidence source_evidence_literature NP470790.RAT1UaChLCqVsUemFg55aRK7cPg1N-gKfP4svz4P_FFPQ130_provenance.
- NP470790.RAT1UaChLCqVsUemFg55aRK7cPg1N-gKfP4svz4P_FFPQ130_assertion SIO_000772 8100831 NP470790.RAT1UaChLCqVsUemFg55aRK7cPg1N-gKfP4svz4P_FFPQ130_provenance.
- NP470790.RAT1UaChLCqVsUemFg55aRK7cPg1N-gKfP4svz4P_FFPQ130_assertion wasDerivedFrom befree-20150227 NP470790.RAT1UaChLCqVsUemFg55aRK7cPg1N-gKfP4svz4P_FFPQ130_provenance.
- NP470790.RAT1UaChLCqVsUemFg55aRK7cPg1N-gKfP4svz4P_FFPQ130_assertion wasGeneratedBy ECO_0000203 NP470790.RAT1UaChLCqVsUemFg55aRK7cPg1N-gKfP4svz4P_FFPQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP470790.RAT1UaChLCqVsUemFg55aRK7cPg1N-gKfP4svz4P_FFPQ130_provenance.