Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP618258.RAakVLDQi7D6VlSob2t4jWVebqIhwHA6I_ScGTISlkCew130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP618258.RAakVLDQi7D6VlSob2t4jWVebqIhwHA6I_ScGTISlkCew130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618258.RAakVLDQi7D6VlSob2t4jWVebqIhwHA6I_ScGTISlkCew130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618258.RAakVLDQi7D6VlSob2t4jWVebqIhwHA6I_ScGTISlkCew130_provenance.
- NP618258.RAakVLDQi7D6VlSob2t4jWVebqIhwHA6I_ScGTISlkCew130_assertion description "[Eight polymorphisms in the promoter of MMP1, MMP2, MMP3, MMP7, MMP9, MMP12, and MMP13 were genotyped in two independent case-control populations; one is from Guangxi province (593 patients with NPC and 480 controls), and the other is from Guangdong province (239 patients and 286 controls).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618258.RAakVLDQi7D6VlSob2t4jWVebqIhwHA6I_ScGTISlkCew130_provenance.
- NP618258.RAakVLDQi7D6VlSob2t4jWVebqIhwHA6I_ScGTISlkCew130_assertion evidence source_evidence_literature NP618258.RAakVLDQi7D6VlSob2t4jWVebqIhwHA6I_ScGTISlkCew130_provenance.
- NP618258.RAakVLDQi7D6VlSob2t4jWVebqIhwHA6I_ScGTISlkCew130_assertion SIO_000772 17607721 NP618258.RAakVLDQi7D6VlSob2t4jWVebqIhwHA6I_ScGTISlkCew130_provenance.
- NP618258.RAakVLDQi7D6VlSob2t4jWVebqIhwHA6I_ScGTISlkCew130_assertion wasDerivedFrom befree-2016 NP618258.RAakVLDQi7D6VlSob2t4jWVebqIhwHA6I_ScGTISlkCew130_provenance.
- NP618258.RAakVLDQi7D6VlSob2t4jWVebqIhwHA6I_ScGTISlkCew130_assertion wasGeneratedBy ECO_0000203 NP618258.RAakVLDQi7D6VlSob2t4jWVebqIhwHA6I_ScGTISlkCew130_provenance.
- befree-2016 importedOn "2016-02-19" NP618258.RAakVLDQi7D6VlSob2t4jWVebqIhwHA6I_ScGTISlkCew130_provenance.