Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP343041.RAtwMgFPzbsjLMYMUNYL3Id8MmNLfkvSZ_K0jMSfnvROI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP343041.RAtwMgFPzbsjLMYMUNYL3Id8MmNLfkvSZ_K0jMSfnvROI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343041.RAtwMgFPzbsjLMYMUNYL3Id8MmNLfkvSZ_K0jMSfnvROI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343041.RAtwMgFPzbsjLMYMUNYL3Id8MmNLfkvSZ_K0jMSfnvROI130_provenance.
- NP343041.RAtwMgFPzbsjLMYMUNYL3Id8MmNLfkvSZ_K0jMSfnvROI130_assertion description "[Combined restriction landmark genomic scanning and virtual genome scans identify a novel human homeobox gene, ALX3, that is hypermethylated in neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343041.RAtwMgFPzbsjLMYMUNYL3Id8MmNLfkvSZ_K0jMSfnvROI130_provenance.
- NP343041.RAtwMgFPzbsjLMYMUNYL3Id8MmNLfkvSZ_K0jMSfnvROI130_assertion evidence source_evidence_literature NP343041.RAtwMgFPzbsjLMYMUNYL3Id8MmNLfkvSZ_K0jMSfnvROI130_provenance.
- NP343041.RAtwMgFPzbsjLMYMUNYL3Id8MmNLfkvSZ_K0jMSfnvROI130_assertion SIO_000772 11807986 NP343041.RAtwMgFPzbsjLMYMUNYL3Id8MmNLfkvSZ_K0jMSfnvROI130_provenance.
- NP343041.RAtwMgFPzbsjLMYMUNYL3Id8MmNLfkvSZ_K0jMSfnvROI130_assertion wasDerivedFrom befree-2016 NP343041.RAtwMgFPzbsjLMYMUNYL3Id8MmNLfkvSZ_K0jMSfnvROI130_provenance.
- NP343041.RAtwMgFPzbsjLMYMUNYL3Id8MmNLfkvSZ_K0jMSfnvROI130_assertion wasGeneratedBy ECO_0000203 NP343041.RAtwMgFPzbsjLMYMUNYL3Id8MmNLfkvSZ_K0jMSfnvROI130_provenance.
- befree-2016 importedOn "2016-02-19" NP343041.RAtwMgFPzbsjLMYMUNYL3Id8MmNLfkvSZ_K0jMSfnvROI130_provenance.