Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP433693.RAHtkVrCPERpbdX_43d1RRW_L0We-glzQ97KXTdTxEkm0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP433693.RAHtkVrCPERpbdX_43d1RRW_L0We-glzQ97KXTdTxEkm0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP433693.RAHtkVrCPERpbdX_43d1RRW_L0We-glzQ97KXTdTxEkm0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP433693.RAHtkVrCPERpbdX_43d1RRW_L0We-glzQ97KXTdTxEkm0130_provenance.
- NP433693.RAHtkVrCPERpbdX_43d1RRW_L0We-glzQ97KXTdTxEkm0130_assertion description "[Furthermore, the mouse homologue (Grb10/Meg1) is reported to be maternally expressed and maps to the imprinted region of proximal mouse chromosome 11 that demonstrates prenatal growth failure when it is maternally disomic.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433693.RAHtkVrCPERpbdX_43d1RRW_L0We-glzQ97KXTdTxEkm0130_provenance.
- NP433693.RAHtkVrCPERpbdX_43d1RRW_L0We-glzQ97KXTdTxEkm0130_assertion evidence source_evidence_literature NP433693.RAHtkVrCPERpbdX_43d1RRW_L0We-glzQ97KXTdTxEkm0130_provenance.
- NP433693.RAHtkVrCPERpbdX_43d1RRW_L0We-glzQ97KXTdTxEkm0130_assertion SIO_000772 10631135 NP433693.RAHtkVrCPERpbdX_43d1RRW_L0We-glzQ97KXTdTxEkm0130_provenance.
- NP433693.RAHtkVrCPERpbdX_43d1RRW_L0We-glzQ97KXTdTxEkm0130_assertion wasDerivedFrom befree-20150227 NP433693.RAHtkVrCPERpbdX_43d1RRW_L0We-glzQ97KXTdTxEkm0130_provenance.
- NP433693.RAHtkVrCPERpbdX_43d1RRW_L0We-glzQ97KXTdTxEkm0130_assertion wasGeneratedBy ECO_0000203 NP433693.RAHtkVrCPERpbdX_43d1RRW_L0We-glzQ97KXTdTxEkm0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP433693.RAHtkVrCPERpbdX_43d1RRW_L0We-glzQ97KXTdTxEkm0130_provenance.