Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP89632.RAsvC72x0GAQ4jAR3Dny2_VHiRPfmZduJxMxAQlHqT_Pc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP89632.RAsvC72x0GAQ4jAR3Dny2_VHiRPfmZduJxMxAQlHqT_Pc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP89632.RAsvC72x0GAQ4jAR3Dny2_VHiRPfmZduJxMxAQlHqT_Pc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP89632.RAsvC72x0GAQ4jAR3Dny2_VHiRPfmZduJxMxAQlHqT_Pc130_provenance.
- NP89632.RAsvC72x0GAQ4jAR3Dny2_VHiRPfmZduJxMxAQlHqT_Pc130_assertion description "[We evaluated the genomic DNA of 241 Alabama white and 124 African American adults who reported no history of hemochromatosis or iron overload to detect HJV missense mutations I222N and G320V using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89632.RAsvC72x0GAQ4jAR3Dny2_VHiRPfmZduJxMxAQlHqT_Pc130_provenance.
- NP89632.RAsvC72x0GAQ4jAR3Dny2_VHiRPfmZduJxMxAQlHqT_Pc130_assertion evidence source_evidence_literature NP89632.RAsvC72x0GAQ4jAR3Dny2_VHiRPfmZduJxMxAQlHqT_Pc130_provenance.
- NP89632.RAsvC72x0GAQ4jAR3Dny2_VHiRPfmZduJxMxAQlHqT_Pc130_assertion SIO_000772 15610558 NP89632.RAsvC72x0GAQ4jAR3Dny2_VHiRPfmZduJxMxAQlHqT_Pc130_provenance.
- NP89632.RAsvC72x0GAQ4jAR3Dny2_VHiRPfmZduJxMxAQlHqT_Pc130_assertion wasDerivedFrom gad-20150221 NP89632.RAsvC72x0GAQ4jAR3Dny2_VHiRPfmZduJxMxAQlHqT_Pc130_provenance.
- NP89632.RAsvC72x0GAQ4jAR3Dny2_VHiRPfmZduJxMxAQlHqT_Pc130_assertion wasGeneratedBy ECO_0000203 NP89632.RAsvC72x0GAQ4jAR3Dny2_VHiRPfmZduJxMxAQlHqT_Pc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP89632.RAsvC72x0GAQ4jAR3Dny2_VHiRPfmZduJxMxAQlHqT_Pc130_provenance.