Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP871510.RA3shWphAQ_HtJURW2U-_n4HC1ZOnXwYe9fcTfKbtFiEw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP871510.RA3shWphAQ_HtJURW2U-_n4HC1ZOnXwYe9fcTfKbtFiEw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP871510.RA3shWphAQ_HtJURW2U-_n4HC1ZOnXwYe9fcTfKbtFiEw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP871510.RA3shWphAQ_HtJURW2U-_n4HC1ZOnXwYe9fcTfKbtFiEw130_provenance.
- NP871510.RA3shWphAQ_HtJURW2U-_n4HC1ZOnXwYe9fcTfKbtFiEw130_assertion description "[CLRN1 mutations cause nonsyndromic retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871510.RA3shWphAQ_HtJURW2U-_n4HC1ZOnXwYe9fcTfKbtFiEw130_provenance.
- NP871510.RA3shWphAQ_HtJURW2U-_n4HC1ZOnXwYe9fcTfKbtFiEw130_assertion evidence source_evidence_literature NP871510.RA3shWphAQ_HtJURW2U-_n4HC1ZOnXwYe9fcTfKbtFiEw130_provenance.
- NP871510.RA3shWphAQ_HtJURW2U-_n4HC1ZOnXwYe9fcTfKbtFiEw130_assertion SIO_000772 21310491 NP871510.RA3shWphAQ_HtJURW2U-_n4HC1ZOnXwYe9fcTfKbtFiEw130_provenance.
- NP871510.RA3shWphAQ_HtJURW2U-_n4HC1ZOnXwYe9fcTfKbtFiEw130_assertion wasDerivedFrom befree-2016 NP871510.RA3shWphAQ_HtJURW2U-_n4HC1ZOnXwYe9fcTfKbtFiEw130_provenance.
- NP871510.RA3shWphAQ_HtJURW2U-_n4HC1ZOnXwYe9fcTfKbtFiEw130_assertion wasGeneratedBy ECO_0000203 NP871510.RA3shWphAQ_HtJURW2U-_n4HC1ZOnXwYe9fcTfKbtFiEw130_provenance.
- befree-2016 importedOn "2016-02-19" NP871510.RA3shWphAQ_HtJURW2U-_n4HC1ZOnXwYe9fcTfKbtFiEw130_provenance.