Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP814980.RAy4HOWBMecwMh1dNbgxL8iF1h7Y4mBsgg8JX4FKJUuYU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP814980.RAy4HOWBMecwMh1dNbgxL8iF1h7Y4mBsgg8JX4FKJUuYU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP814980.RAy4HOWBMecwMh1dNbgxL8iF1h7Y4mBsgg8JX4FKJUuYU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP814980.RAy4HOWBMecwMh1dNbgxL8iF1h7Y4mBsgg8JX4FKJUuYU130_provenance.
- NP814980.RAy4HOWBMecwMh1dNbgxL8iF1h7Y4mBsgg8JX4FKJUuYU130_assertion description "[ARS shows great clinical variability and encompasses several conditions with overlapping phenotypes, including Rieger syndrome (RS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP814980.RAy4HOWBMecwMh1dNbgxL8iF1h7Y4mBsgg8JX4FKJUuYU130_provenance.
- NP814980.RAy4HOWBMecwMh1dNbgxL8iF1h7Y4mBsgg8JX4FKJUuYU130_assertion evidence source_evidence_literature NP814980.RAy4HOWBMecwMh1dNbgxL8iF1h7Y4mBsgg8JX4FKJUuYU130_provenance.
- NP814980.RAy4HOWBMecwMh1dNbgxL8iF1h7Y4mBsgg8JX4FKJUuYU130_assertion SIO_000772 17850355 NP814980.RAy4HOWBMecwMh1dNbgxL8iF1h7Y4mBsgg8JX4FKJUuYU130_provenance.
- NP814980.RAy4HOWBMecwMh1dNbgxL8iF1h7Y4mBsgg8JX4FKJUuYU130_assertion wasDerivedFrom befree-20140225 NP814980.RAy4HOWBMecwMh1dNbgxL8iF1h7Y4mBsgg8JX4FKJUuYU130_provenance.
- NP814980.RAy4HOWBMecwMh1dNbgxL8iF1h7Y4mBsgg8JX4FKJUuYU130_assertion wasGeneratedBy ECO_0000203 NP814980.RAy4HOWBMecwMh1dNbgxL8iF1h7Y4mBsgg8JX4FKJUuYU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP814980.RAy4HOWBMecwMh1dNbgxL8iF1h7Y4mBsgg8JX4FKJUuYU130_provenance.