Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP243876.RA2_PJ2hR50CzKV0xnOhIZa6BrRV6Op7P3qIBa4cN6O18130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP243876.RA2_PJ2hR50CzKV0xnOhIZa6BrRV6Op7P3qIBa4cN6O18130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP243876.RA2_PJ2hR50CzKV0xnOhIZa6BrRV6Op7P3qIBa4cN6O18130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP243876.RA2_PJ2hR50CzKV0xnOhIZa6BrRV6Op7P3qIBa4cN6O18130_provenance.
- NP243876.RA2_PJ2hR50CzKV0xnOhIZa6BrRV6Op7P3qIBa4cN6O18130_assertion wasGeneratedBy ECO_0000203 NP243876.RA2_PJ2hR50CzKV0xnOhIZa6BrRV6Op7P3qIBa4cN6O18130_provenance.
- NP243876.RA2_PJ2hR50CzKV0xnOhIZa6BrRV6Op7P3qIBa4cN6O18130_assertion wasDerivedFrom befree-20140225 NP243876.RA2_PJ2hR50CzKV0xnOhIZa6BrRV6Op7P3qIBa4cN6O18130_provenance.
- NP243876.RA2_PJ2hR50CzKV0xnOhIZa6BrRV6Op7P3qIBa4cN6O18130_assertion SIO_000772 11545688 NP243876.RA2_PJ2hR50CzKV0xnOhIZa6BrRV6Op7P3qIBa4cN6O18130_provenance.
- NP243876.RA2_PJ2hR50CzKV0xnOhIZa6BrRV6Op7P3qIBa4cN6O18130_assertion evidence source_evidence_literature NP243876.RA2_PJ2hR50CzKV0xnOhIZa6BrRV6Op7P3qIBa4cN6O18130_provenance.
- NP243876.RA2_PJ2hR50CzKV0xnOhIZa6BrRV6Op7P3qIBa4cN6O18130_assertion description "[TCC is allelic to SYM1, and at least two different mutations in NOG can result in either TCC or SYM1 in different families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243876.RA2_PJ2hR50CzKV0xnOhIZa6BrRV6Op7P3qIBa4cN6O18130_provenance.
- befree-20140225 importedOn "2014-02-25" NP243876.RA2_PJ2hR50CzKV0xnOhIZa6BrRV6Op7P3qIBa4cN6O18130_provenance.