Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP51512.RA6POEN8SYl8mku49kZAmIxnThd8gCG4f4kRHDA3WiGZ4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP51512.RA6POEN8SYl8mku49kZAmIxnThd8gCG4f4kRHDA3WiGZ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP51512.RA6POEN8SYl8mku49kZAmIxnThd8gCG4f4kRHDA3WiGZ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP51512.RA6POEN8SYl8mku49kZAmIxnThd8gCG4f4kRHDA3WiGZ4130_provenance.
- NP51512.RA6POEN8SYl8mku49kZAmIxnThd8gCG4f4kRHDA3WiGZ4130_assertion description "[Prospective variants screening of connexin genes in children with hearing impairment: genotype/phenotype correlation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51512.RA6POEN8SYl8mku49kZAmIxnThd8gCG4f4kRHDA3WiGZ4130_provenance.
- NP51512.RA6POEN8SYl8mku49kZAmIxnThd8gCG4f4kRHDA3WiGZ4130_assertion evidence source_evidence_literature NP51512.RA6POEN8SYl8mku49kZAmIxnThd8gCG4f4kRHDA3WiGZ4130_provenance.
- NP51512.RA6POEN8SYl8mku49kZAmIxnThd8gCG4f4kRHDA3WiGZ4130_assertion SIO_000772 20593197 NP51512.RA6POEN8SYl8mku49kZAmIxnThd8gCG4f4kRHDA3WiGZ4130_provenance.
- NP51512.RA6POEN8SYl8mku49kZAmIxnThd8gCG4f4kRHDA3WiGZ4130_assertion wasDerivedFrom gad-20150221 NP51512.RA6POEN8SYl8mku49kZAmIxnThd8gCG4f4kRHDA3WiGZ4130_provenance.
- NP51512.RA6POEN8SYl8mku49kZAmIxnThd8gCG4f4kRHDA3WiGZ4130_assertion wasGeneratedBy ECO_0000203 NP51512.RA6POEN8SYl8mku49kZAmIxnThd8gCG4f4kRHDA3WiGZ4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP51512.RA6POEN8SYl8mku49kZAmIxnThd8gCG4f4kRHDA3WiGZ4130_provenance.