Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP719662.RAyXiAl3KYZOtrsHI_0nASkqgAuPyYLZvtSKahoGSoHuo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP719662.RAyXiAl3KYZOtrsHI_0nASkqgAuPyYLZvtSKahoGSoHuo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719662.RAyXiAl3KYZOtrsHI_0nASkqgAuPyYLZvtSKahoGSoHuo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719662.RAyXiAl3KYZOtrsHI_0nASkqgAuPyYLZvtSKahoGSoHuo130_provenance.
- NP719662.RAyXiAl3KYZOtrsHI_0nASkqgAuPyYLZvtSKahoGSoHuo130_assertion description "[We used two highly informative (CA)n repeats, D9S126 and IFNA, previously implicated in familial malignant melanoma (MLM), to conduct linkage analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719662.RAyXiAl3KYZOtrsHI_0nASkqgAuPyYLZvtSKahoGSoHuo130_provenance.
- NP719662.RAyXiAl3KYZOtrsHI_0nASkqgAuPyYLZvtSKahoGSoHuo130_assertion evidence source_evidence_literature NP719662.RAyXiAl3KYZOtrsHI_0nASkqgAuPyYLZvtSKahoGSoHuo130_provenance.
- NP719662.RAyXiAl3KYZOtrsHI_0nASkqgAuPyYLZvtSKahoGSoHuo130_assertion SIO_000772 8116618 NP719662.RAyXiAl3KYZOtrsHI_0nASkqgAuPyYLZvtSKahoGSoHuo130_provenance.
- NP719662.RAyXiAl3KYZOtrsHI_0nASkqgAuPyYLZvtSKahoGSoHuo130_assertion wasDerivedFrom befree-20140225 NP719662.RAyXiAl3KYZOtrsHI_0nASkqgAuPyYLZvtSKahoGSoHuo130_provenance.
- NP719662.RAyXiAl3KYZOtrsHI_0nASkqgAuPyYLZvtSKahoGSoHuo130_assertion wasGeneratedBy ECO_0000203 NP719662.RAyXiAl3KYZOtrsHI_0nASkqgAuPyYLZvtSKahoGSoHuo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP719662.RAyXiAl3KYZOtrsHI_0nASkqgAuPyYLZvtSKahoGSoHuo130_provenance.