Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP177503.RAEeZkyzEL9LuFXFc37tEMFw1HHXJ_xPbrQSemrHNUG64130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP177503.RAEeZkyzEL9LuFXFc37tEMFw1HHXJ_xPbrQSemrHNUG64130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP177503.RAEeZkyzEL9LuFXFc37tEMFw1HHXJ_xPbrQSemrHNUG64130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP177503.RAEeZkyzEL9LuFXFc37tEMFw1HHXJ_xPbrQSemrHNUG64130_provenance.
- NP177503.RAEeZkyzEL9LuFXFc37tEMFw1HHXJ_xPbrQSemrHNUG64130_assertion description "[High incidence of loss of heterozygosity and abnormal imprinting of H19 and IGF2 genes in invasive cervical carcinomas. Uncoupling of H19 and IGF2 expression and biallelic hypomethylation of H19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177503.RAEeZkyzEL9LuFXFc37tEMFw1HHXJ_xPbrQSemrHNUG64130_provenance.
- NP177503.RAEeZkyzEL9LuFXFc37tEMFw1HHXJ_xPbrQSemrHNUG64130_assertion evidence source_evidence_literature NP177503.RAEeZkyzEL9LuFXFc37tEMFw1HHXJ_xPbrQSemrHNUG64130_provenance.
- NP177503.RAEeZkyzEL9LuFXFc37tEMFw1HHXJ_xPbrQSemrHNUG64130_assertion SIO_000772 8570220 NP177503.RAEeZkyzEL9LuFXFc37tEMFw1HHXJ_xPbrQSemrHNUG64130_provenance.
- NP177503.RAEeZkyzEL9LuFXFc37tEMFw1HHXJ_xPbrQSemrHNUG64130_assertion wasDerivedFrom befree-20140225 NP177503.RAEeZkyzEL9LuFXFc37tEMFw1HHXJ_xPbrQSemrHNUG64130_provenance.
- NP177503.RAEeZkyzEL9LuFXFc37tEMFw1HHXJ_xPbrQSemrHNUG64130_assertion wasGeneratedBy ECO_0000203 NP177503.RAEeZkyzEL9LuFXFc37tEMFw1HHXJ_xPbrQSemrHNUG64130_provenance.
- befree-20140225 importedOn "2014-02-25" NP177503.RAEeZkyzEL9LuFXFc37tEMFw1HHXJ_xPbrQSemrHNUG64130_provenance.