Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP778008.RA-nw-sfD1zK3TDbm0WSWPFR4eC0gBIxoOznPxcadSPnU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP778008.RA-nw-sfD1zK3TDbm0WSWPFR4eC0gBIxoOznPxcadSPnU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778008.RA-nw-sfD1zK3TDbm0WSWPFR4eC0gBIxoOznPxcadSPnU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778008.RA-nw-sfD1zK3TDbm0WSWPFR4eC0gBIxoOznPxcadSPnU130_provenance.
- NP778008.RA-nw-sfD1zK3TDbm0WSWPFR4eC0gBIxoOznPxcadSPnU130_assertion description "[The excellent response to therapy of early identified patients with GAMT or AGAT deficiency candidates these condition for inclusion in newborn screening programs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778008.RA-nw-sfD1zK3TDbm0WSWPFR4eC0gBIxoOznPxcadSPnU130_provenance.
- NP778008.RA-nw-sfD1zK3TDbm0WSWPFR4eC0gBIxoOznPxcadSPnU130_assertion evidence source_evidence_literature NP778008.RA-nw-sfD1zK3TDbm0WSWPFR4eC0gBIxoOznPxcadSPnU130_provenance.
- NP778008.RA-nw-sfD1zK3TDbm0WSWPFR4eC0gBIxoOznPxcadSPnU130_assertion SIO_000772 21308988 NP778008.RA-nw-sfD1zK3TDbm0WSWPFR4eC0gBIxoOznPxcadSPnU130_provenance.
- NP778008.RA-nw-sfD1zK3TDbm0WSWPFR4eC0gBIxoOznPxcadSPnU130_assertion wasDerivedFrom befree-20140225 NP778008.RA-nw-sfD1zK3TDbm0WSWPFR4eC0gBIxoOznPxcadSPnU130_provenance.
- NP778008.RA-nw-sfD1zK3TDbm0WSWPFR4eC0gBIxoOznPxcadSPnU130_assertion wasGeneratedBy ECO_0000203 NP778008.RA-nw-sfD1zK3TDbm0WSWPFR4eC0gBIxoOznPxcadSPnU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP778008.RA-nw-sfD1zK3TDbm0WSWPFR4eC0gBIxoOznPxcadSPnU130_provenance.