Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP178779.RAb3hJ-_nA-pvL5GPnHxgyzfV12HpL8a7WMY6Cr_-6NGg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP178779.RAb3hJ-_nA-pvL5GPnHxgyzfV12HpL8a7WMY6Cr_-6NGg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP178779.RAb3hJ-_nA-pvL5GPnHxgyzfV12HpL8a7WMY6Cr_-6NGg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP178779.RAb3hJ-_nA-pvL5GPnHxgyzfV12HpL8a7WMY6Cr_-6NGg130_provenance.
- NP178779.RAb3hJ-_nA-pvL5GPnHxgyzfV12HpL8a7WMY6Cr_-6NGg130_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." NP178779.RAb3hJ-_nA-pvL5GPnHxgyzfV12HpL8a7WMY6Cr_-6NGg130_provenance.
- NP178779.RAb3hJ-_nA-pvL5GPnHxgyzfV12HpL8a7WMY6Cr_-6NGg130_assertion evidence source_evidence_literature NP178779.RAb3hJ-_nA-pvL5GPnHxgyzfV12HpL8a7WMY6Cr_-6NGg130_provenance.
- NP178779.RAb3hJ-_nA-pvL5GPnHxgyzfV12HpL8a7WMY6Cr_-6NGg130_assertion SIO_000772 19432826 NP178779.RAb3hJ-_nA-pvL5GPnHxgyzfV12HpL8a7WMY6Cr_-6NGg130_provenance.
- NP178779.RAb3hJ-_nA-pvL5GPnHxgyzfV12HpL8a7WMY6Cr_-6NGg130_assertion wasDerivedFrom befree-20140225 NP178779.RAb3hJ-_nA-pvL5GPnHxgyzfV12HpL8a7WMY6Cr_-6NGg130_provenance.
- NP178779.RAb3hJ-_nA-pvL5GPnHxgyzfV12HpL8a7WMY6Cr_-6NGg130_assertion wasGeneratedBy ECO_0000203 NP178779.RAb3hJ-_nA-pvL5GPnHxgyzfV12HpL8a7WMY6Cr_-6NGg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP178779.RAb3hJ-_nA-pvL5GPnHxgyzfV12HpL8a7WMY6Cr_-6NGg130_provenance.