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- source_evidence_literature type ECO_0000212 NP183235.RALTrm0Nk15XSvaKproNVdvJ97-OZItfJ-Ft3kwux91BU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183235.RALTrm0Nk15XSvaKproNVdvJ97-OZItfJ-Ft3kwux91BU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183235.RALTrm0Nk15XSvaKproNVdvJ97-OZItfJ-Ft3kwux91BU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP183235.RALTrm0Nk15XSvaKproNVdvJ97-OZItfJ-Ft3kwux91BU130_provenance.
- NP183235.RALTrm0Nk15XSvaKproNVdvJ97-OZItfJ-Ft3kwux91BU130_assertion wasGeneratedBy ECO_0000203 NP183235.RALTrm0Nk15XSvaKproNVdvJ97-OZItfJ-Ft3kwux91BU130_provenance.
- NP183235.RALTrm0Nk15XSvaKproNVdvJ97-OZItfJ-Ft3kwux91BU130_assertion wasDerivedFrom gad-20150221 NP183235.RALTrm0Nk15XSvaKproNVdvJ97-OZItfJ-Ft3kwux91BU130_provenance.
- NP183235.RALTrm0Nk15XSvaKproNVdvJ97-OZItfJ-Ft3kwux91BU130_assertion SIO_000772 20687945 NP183235.RALTrm0Nk15XSvaKproNVdvJ97-OZItfJ-Ft3kwux91BU130_provenance.
- NP183235.RALTrm0Nk15XSvaKproNVdvJ97-OZItfJ-Ft3kwux91BU130_assertion evidence source_evidence_literature NP183235.RALTrm0Nk15XSvaKproNVdvJ97-OZItfJ-Ft3kwux91BU130_provenance.
- NP183235.RALTrm0Nk15XSvaKproNVdvJ97-OZItfJ-Ft3kwux91BU130_assertion description "[Here, we describe a screening method, HRM, for the detection of both heterozygous and homozygous mutations in the gene encoding MUTYH in selected samples of patients with phenotype of MAP. We refine the capabilities of HRM-PCR and apply it to a gene not y]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183235.RALTrm0Nk15XSvaKproNVdvJ97-OZItfJ-Ft3kwux91BU130_provenance.