Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1232332.RAvli5AB1uwpYhZa0XWmme-htj5P4NfGt7Oa9KJ2vBelg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1232332.RAvli5AB1uwpYhZa0XWmme-htj5P4NfGt7Oa9KJ2vBelg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1232332.RAvli5AB1uwpYhZa0XWmme-htj5P4NfGt7Oa9KJ2vBelg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1232332.RAvli5AB1uwpYhZa0XWmme-htj5P4NfGt7Oa9KJ2vBelg130_provenance.
- NP1232332.RAvli5AB1uwpYhZa0XWmme-htj5P4NfGt7Oa9KJ2vBelg130_assertion description "[PAX6 mutations may be associated with diverse clinical features ranging from severely impaired ocular and pituitary development to apparently normal phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232332.RAvli5AB1uwpYhZa0XWmme-htj5P4NfGt7Oa9KJ2vBelg130_provenance.
- NP1232332.RAvli5AB1uwpYhZa0XWmme-htj5P4NfGt7Oa9KJ2vBelg130_assertion evidence source_evidence_literature NP1232332.RAvli5AB1uwpYhZa0XWmme-htj5P4NfGt7Oa9KJ2vBelg130_provenance.
- NP1232332.RAvli5AB1uwpYhZa0XWmme-htj5P4NfGt7Oa9KJ2vBelg130_assertion SIO_000772 25342853 NP1232332.RAvli5AB1uwpYhZa0XWmme-htj5P4NfGt7Oa9KJ2vBelg130_provenance.
- NP1232332.RAvli5AB1uwpYhZa0XWmme-htj5P4NfGt7Oa9KJ2vBelg130_assertion wasDerivedFrom befree-2016 NP1232332.RAvli5AB1uwpYhZa0XWmme-htj5P4NfGt7Oa9KJ2vBelg130_provenance.
- NP1232332.RAvli5AB1uwpYhZa0XWmme-htj5P4NfGt7Oa9KJ2vBelg130_assertion wasGeneratedBy ECO_0000203 NP1232332.RAvli5AB1uwpYhZa0XWmme-htj5P4NfGt7Oa9KJ2vBelg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1232332.RAvli5AB1uwpYhZa0XWmme-htj5P4NfGt7Oa9KJ2vBelg130_provenance.