Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP811318.RAFQeKYfR5rgfMjXJnmlRH0PcGpWhkz_lowgajuGd0miw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP811318.RAFQeKYfR5rgfMjXJnmlRH0PcGpWhkz_lowgajuGd0miw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP811318.RAFQeKYfR5rgfMjXJnmlRH0PcGpWhkz_lowgajuGd0miw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP811318.RAFQeKYfR5rgfMjXJnmlRH0PcGpWhkz_lowgajuGd0miw130_provenance.
- NP811318.RAFQeKYfR5rgfMjXJnmlRH0PcGpWhkz_lowgajuGd0miw130_assertion description "[This contig, which has on average fourfold clone coverage, was assembled by STS and EST content analysis using 46 markers, including 8 ESTs, two retinally expressed genes, and 22 new STSs developed from BAC- and PAC-derived DNA sequence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811318.RAFQeKYfR5rgfMjXJnmlRH0PcGpWhkz_lowgajuGd0miw130_provenance.
- NP811318.RAFQeKYfR5rgfMjXJnmlRH0PcGpWhkz_lowgajuGd0miw130_assertion evidence source_evidence_literature NP811318.RAFQeKYfR5rgfMjXJnmlRH0PcGpWhkz_lowgajuGd0miw130_provenance.
- NP811318.RAFQeKYfR5rgfMjXJnmlRH0PcGpWhkz_lowgajuGd0miw130_assertion SIO_000772 10950933 NP811318.RAFQeKYfR5rgfMjXJnmlRH0PcGpWhkz_lowgajuGd0miw130_provenance.
- NP811318.RAFQeKYfR5rgfMjXJnmlRH0PcGpWhkz_lowgajuGd0miw130_assertion wasDerivedFrom befree-20140225 NP811318.RAFQeKYfR5rgfMjXJnmlRH0PcGpWhkz_lowgajuGd0miw130_provenance.
- NP811318.RAFQeKYfR5rgfMjXJnmlRH0PcGpWhkz_lowgajuGd0miw130_assertion wasGeneratedBy ECO_0000203 NP811318.RAFQeKYfR5rgfMjXJnmlRH0PcGpWhkz_lowgajuGd0miw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP811318.RAFQeKYfR5rgfMjXJnmlRH0PcGpWhkz_lowgajuGd0miw130_provenance.