Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP92836.RAPJpPliiYDWDI_U3lQh1Mh3GhbCPbmVrIgWir4DC7Yho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP92836.RAPJpPliiYDWDI_U3lQh1Mh3GhbCPbmVrIgWir4DC7Yho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP92836.RAPJpPliiYDWDI_U3lQh1Mh3GhbCPbmVrIgWir4DC7Yho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP92836.RAPJpPliiYDWDI_U3lQh1Mh3GhbCPbmVrIgWir4DC7Yho130_provenance.
- NP92836.RAPJpPliiYDWDI_U3lQh1Mh3GhbCPbmVrIgWir4DC7Yho130_assertion description "[Association of MMP1, MMP3, MMP9, and MMP12 polymorphisms with risk and clinical course of multiple sclerosis in a Polish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92836.RAPJpPliiYDWDI_U3lQh1Mh3GhbCPbmVrIgWir4DC7Yho130_provenance.
- NP92836.RAPJpPliiYDWDI_U3lQh1Mh3GhbCPbmVrIgWir4DC7Yho130_assertion evidence source_evidence_literature NP92836.RAPJpPliiYDWDI_U3lQh1Mh3GhbCPbmVrIgWir4DC7Yho130_provenance.
- NP92836.RAPJpPliiYDWDI_U3lQh1Mh3GhbCPbmVrIgWir4DC7Yho130_assertion SIO_000772 19628284 NP92836.RAPJpPliiYDWDI_U3lQh1Mh3GhbCPbmVrIgWir4DC7Yho130_provenance.
- NP92836.RAPJpPliiYDWDI_U3lQh1Mh3GhbCPbmVrIgWir4DC7Yho130_assertion wasDerivedFrom gad-20150221 NP92836.RAPJpPliiYDWDI_U3lQh1Mh3GhbCPbmVrIgWir4DC7Yho130_provenance.
- NP92836.RAPJpPliiYDWDI_U3lQh1Mh3GhbCPbmVrIgWir4DC7Yho130_assertion wasGeneratedBy ECO_0000203 NP92836.RAPJpPliiYDWDI_U3lQh1Mh3GhbCPbmVrIgWir4DC7Yho130_provenance.
- gad-20150221 importedOn "2015-02-21" NP92836.RAPJpPliiYDWDI_U3lQh1Mh3GhbCPbmVrIgWir4DC7Yho130_provenance.