Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP713842.RAIqBA8uEFWXm4dPDYQYUtFvqqR0c1U457tIG7zycHwW0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP713842.RAIqBA8uEFWXm4dPDYQYUtFvqqR0c1U457tIG7zycHwW0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP713842.RAIqBA8uEFWXm4dPDYQYUtFvqqR0c1U457tIG7zycHwW0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP713842.RAIqBA8uEFWXm4dPDYQYUtFvqqR0c1U457tIG7zycHwW0130_provenance.
- NP713842.RAIqBA8uEFWXm4dPDYQYUtFvqqR0c1U457tIG7zycHwW0130_assertion description "[Single nucleotide polymorphisms in human MMP genes, including MMP1 (-1637 1G>2G), MMP3 (-1612 5A>6A), MMP9 (-1562 C>T), and MMP12 (-82 A>G), and their impact on multiple sclerosis risk and disease progression in a Polish population were investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713842.RAIqBA8uEFWXm4dPDYQYUtFvqqR0c1U457tIG7zycHwW0130_provenance.
- NP713842.RAIqBA8uEFWXm4dPDYQYUtFvqqR0c1U457tIG7zycHwW0130_assertion evidence source_evidence_literature NP713842.RAIqBA8uEFWXm4dPDYQYUtFvqqR0c1U457tIG7zycHwW0130_provenance.
- NP713842.RAIqBA8uEFWXm4dPDYQYUtFvqqR0c1U457tIG7zycHwW0130_assertion SIO_000772 19628284 NP713842.RAIqBA8uEFWXm4dPDYQYUtFvqqR0c1U457tIG7zycHwW0130_provenance.
- NP713842.RAIqBA8uEFWXm4dPDYQYUtFvqqR0c1U457tIG7zycHwW0130_assertion wasDerivedFrom befree-20140225 NP713842.RAIqBA8uEFWXm4dPDYQYUtFvqqR0c1U457tIG7zycHwW0130_provenance.
- NP713842.RAIqBA8uEFWXm4dPDYQYUtFvqqR0c1U457tIG7zycHwW0130_assertion wasGeneratedBy ECO_0000203 NP713842.RAIqBA8uEFWXm4dPDYQYUtFvqqR0c1U457tIG7zycHwW0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP713842.RAIqBA8uEFWXm4dPDYQYUtFvqqR0c1U457tIG7zycHwW0130_provenance.