Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1358396.RAQWN_KltUJiAV-vCxRkoz8pqEnqOn6gB8v-hIHU88Iw0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1358396.RAQWN_KltUJiAV-vCxRkoz8pqEnqOn6gB8v-hIHU88Iw0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1358396.RAQWN_KltUJiAV-vCxRkoz8pqEnqOn6gB8v-hIHU88Iw0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1358396.RAQWN_KltUJiAV-vCxRkoz8pqEnqOn6gB8v-hIHU88Iw0130_provenance.
- NP1358396.RAQWN_KltUJiAV-vCxRkoz8pqEnqOn6gB8v-hIHU88Iw0130_assertion description "[We report on the allele distributions in a normal black African population at two microsatellite loci neighbouring the FRAXA locus and at the CGG repeat in the 5' end of the FMR-1 gene, which causes the fragile X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1358396.RAQWN_KltUJiAV-vCxRkoz8pqEnqOn6gB8v-hIHU88Iw0130_provenance.
- NP1358396.RAQWN_KltUJiAV-vCxRkoz8pqEnqOn6gB8v-hIHU88Iw0130_assertion evidence source_evidence_literature NP1358396.RAQWN_KltUJiAV-vCxRkoz8pqEnqOn6gB8v-hIHU88Iw0130_provenance.
- NP1358396.RAQWN_KltUJiAV-vCxRkoz8pqEnqOn6gB8v-hIHU88Iw0130_assertion SIO_000772 8826479 NP1358396.RAQWN_KltUJiAV-vCxRkoz8pqEnqOn6gB8v-hIHU88Iw0130_provenance.
- NP1358396.RAQWN_KltUJiAV-vCxRkoz8pqEnqOn6gB8v-hIHU88Iw0130_assertion wasDerivedFrom befree-2016 NP1358396.RAQWN_KltUJiAV-vCxRkoz8pqEnqOn6gB8v-hIHU88Iw0130_provenance.
- NP1358396.RAQWN_KltUJiAV-vCxRkoz8pqEnqOn6gB8v-hIHU88Iw0130_assertion wasGeneratedBy ECO_0000203 NP1358396.RAQWN_KltUJiAV-vCxRkoz8pqEnqOn6gB8v-hIHU88Iw0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1358396.RAQWN_KltUJiAV-vCxRkoz8pqEnqOn6gB8v-hIHU88Iw0130_provenance.