Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP726199.RAOu6wWPGGPqbvCs08cWSlRTPaa61lic0PK6ZtVfKPMGI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP726199.RAOu6wWPGGPqbvCs08cWSlRTPaa61lic0PK6ZtVfKPMGI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP726199.RAOu6wWPGGPqbvCs08cWSlRTPaa61lic0PK6ZtVfKPMGI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP726199.RAOu6wWPGGPqbvCs08cWSlRTPaa61lic0PK6ZtVfKPMGI130_provenance.
- NP726199.RAOu6wWPGGPqbvCs08cWSlRTPaa61lic0PK6ZtVfKPMGI130_assertion description "[One patient with OFC syndrome carried a large deletion of the EYA1 gene region, confirming that OFC syndrome is allelic with BOR syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP726199.RAOu6wWPGGPqbvCs08cWSlRTPaa61lic0PK6ZtVfKPMGI130_provenance.
- NP726199.RAOu6wWPGGPqbvCs08cWSlRTPaa61lic0PK6ZtVfKPMGI130_assertion evidence source_evidence_literature NP726199.RAOu6wWPGGPqbvCs08cWSlRTPaa61lic0PK6ZtVfKPMGI130_provenance.
- NP726199.RAOu6wWPGGPqbvCs08cWSlRTPaa61lic0PK6ZtVfKPMGI130_assertion SIO_000772 11409867 NP726199.RAOu6wWPGGPqbvCs08cWSlRTPaa61lic0PK6ZtVfKPMGI130_provenance.
- NP726199.RAOu6wWPGGPqbvCs08cWSlRTPaa61lic0PK6ZtVfKPMGI130_assertion wasDerivedFrom befree-20140225 NP726199.RAOu6wWPGGPqbvCs08cWSlRTPaa61lic0PK6ZtVfKPMGI130_provenance.
- NP726199.RAOu6wWPGGPqbvCs08cWSlRTPaa61lic0PK6ZtVfKPMGI130_assertion wasGeneratedBy ECO_0000203 NP726199.RAOu6wWPGGPqbvCs08cWSlRTPaa61lic0PK6ZtVfKPMGI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP726199.RAOu6wWPGGPqbvCs08cWSlRTPaa61lic0PK6ZtVfKPMGI130_provenance.