Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance.
- NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_assertion wasGeneratedBy ECO_0000203 NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance.
- NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_assertion wasDerivedFrom befree-2016 NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance.
- NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_assertion SIO_000772 8058286 NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance.
- NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_assertion evidence source_evidence_literature NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance.
- NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_assertion description "[Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance.