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- source_evidence_literature type ECO_0000212 NP738012.RAb5md9Yu1HdZXZQfVEidanTGG83gmerTlpRFCy81T9l0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP738012.RAb5md9Yu1HdZXZQfVEidanTGG83gmerTlpRFCy81T9l0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP738012.RAb5md9Yu1HdZXZQfVEidanTGG83gmerTlpRFCy81T9l0130_provenance.
- NP738012.RAb5md9Yu1HdZXZQfVEidanTGG83gmerTlpRFCy81T9l0130_assertion description "[The major genetic risk factor in our series of patients was homozygosity for the MTHFR C677T mutation (7 out of 48 patients); three more patients were found to be heterozygous for the Factor V Leiden mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP738012.RAb5md9Yu1HdZXZQfVEidanTGG83gmerTlpRFCy81T9l0130_provenance.
- NP738012.RAb5md9Yu1HdZXZQfVEidanTGG83gmerTlpRFCy81T9l0130_assertion evidence source_evidence_literature NP738012.RAb5md9Yu1HdZXZQfVEidanTGG83gmerTlpRFCy81T9l0130_provenance.
- NP738012.RAb5md9Yu1HdZXZQfVEidanTGG83gmerTlpRFCy81T9l0130_assertion SIO_000772 19432826 NP738012.RAb5md9Yu1HdZXZQfVEidanTGG83gmerTlpRFCy81T9l0130_provenance.
- NP738012.RAb5md9Yu1HdZXZQfVEidanTGG83gmerTlpRFCy81T9l0130_assertion wasDerivedFrom befree-2016 NP738012.RAb5md9Yu1HdZXZQfVEidanTGG83gmerTlpRFCy81T9l0130_provenance.
- NP738012.RAb5md9Yu1HdZXZQfVEidanTGG83gmerTlpRFCy81T9l0130_assertion wasGeneratedBy ECO_0000203 NP738012.RAb5md9Yu1HdZXZQfVEidanTGG83gmerTlpRFCy81T9l0130_provenance.
- befree-2016 importedOn "2016-02-19" NP738012.RAb5md9Yu1HdZXZQfVEidanTGG83gmerTlpRFCy81T9l0130_provenance.