Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP521104.RAgmjE2mpBfBFxSN7LLxFd0QoCWS_bKTdVblh-e1mYz2k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP521104.RAgmjE2mpBfBFxSN7LLxFd0QoCWS_bKTdVblh-e1mYz2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP521104.RAgmjE2mpBfBFxSN7LLxFd0QoCWS_bKTdVblh-e1mYz2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP521104.RAgmjE2mpBfBFxSN7LLxFd0QoCWS_bKTdVblh-e1mYz2k130_provenance.
- NP521104.RAgmjE2mpBfBFxSN7LLxFd0QoCWS_bKTdVblh-e1mYz2k130_assertion description "[The deletion breakpoints were precisely identified for each deletion and primers were designed in the unique regions across the breakpoints of HPFH-1 (Black), HPFH-2 (Ghanaian), HPFH-3 (Asian Indian), HPFH-4 (Italian), HPFH-5 (Italian), HPFH-6 (Vietnamese), HPFH-7 (Kenyan), and SEA-HPFH (Southeast Asian).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521104.RAgmjE2mpBfBFxSN7LLxFd0QoCWS_bKTdVblh-e1mYz2k130_provenance.
- NP521104.RAgmjE2mpBfBFxSN7LLxFd0QoCWS_bKTdVblh-e1mYz2k130_assertion evidence source_evidence_literature NP521104.RAgmjE2mpBfBFxSN7LLxFd0QoCWS_bKTdVblh-e1mYz2k130_provenance.
- NP521104.RAgmjE2mpBfBFxSN7LLxFd0QoCWS_bKTdVblh-e1mYz2k130_assertion SIO_000772 16271016 NP521104.RAgmjE2mpBfBFxSN7LLxFd0QoCWS_bKTdVblh-e1mYz2k130_provenance.
- NP521104.RAgmjE2mpBfBFxSN7LLxFd0QoCWS_bKTdVblh-e1mYz2k130_assertion wasDerivedFrom befree-2016 NP521104.RAgmjE2mpBfBFxSN7LLxFd0QoCWS_bKTdVblh-e1mYz2k130_provenance.
- NP521104.RAgmjE2mpBfBFxSN7LLxFd0QoCWS_bKTdVblh-e1mYz2k130_assertion wasGeneratedBy ECO_0000203 NP521104.RAgmjE2mpBfBFxSN7LLxFd0QoCWS_bKTdVblh-e1mYz2k130_provenance.
- befree-2016 importedOn "2016-02-19" NP521104.RAgmjE2mpBfBFxSN7LLxFd0QoCWS_bKTdVblh-e1mYz2k130_provenance.