Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP574313.RA9v71StRKkdfNrDA0nGFBs_PC9Ba_zANUxHjhH3VaQ-E130_assertion> ?p ?o ?g. }
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- NP574313.RA9v71StRKkdfNrDA0nGFBs_PC9Ba_zANUxHjhH3VaQ-E130_assertion type Assertion NP574313.RA9v71StRKkdfNrDA0nGFBs_PC9Ba_zANUxHjhH3VaQ-E130_head.
- NP574313.RA9v71StRKkdfNrDA0nGFBs_PC9Ba_zANUxHjhH3VaQ-E130_assertion description "[The prevalence of the factor V Leiden mutation (FVL) and the prothrombin G20210A mutation and of homozygosity for the methylenetetrahydrofolate reductase (MTHFR) C677T substitution has been analyzed in a cohort of 175 patients with gastrointestinal adenocarcinoma by the polymerase chain reaction-restriction fragment length polymorphism technique.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP574313.RA9v71StRKkdfNrDA0nGFBs_PC9Ba_zANUxHjhH3VaQ-E130_provenance.
- NP574313.RA9v71StRKkdfNrDA0nGFBs_PC9Ba_zANUxHjhH3VaQ-E130_assertion evidence source_evidence_literature NP574313.RA9v71StRKkdfNrDA0nGFBs_PC9Ba_zANUxHjhH3VaQ-E130_provenance.
- NP574313.RA9v71StRKkdfNrDA0nGFBs_PC9Ba_zANUxHjhH3VaQ-E130_assertion SIO_000772 12115343 NP574313.RA9v71StRKkdfNrDA0nGFBs_PC9Ba_zANUxHjhH3VaQ-E130_provenance.
- NP574313.RA9v71StRKkdfNrDA0nGFBs_PC9Ba_zANUxHjhH3VaQ-E130_assertion wasDerivedFrom befree-20150227 NP574313.RA9v71StRKkdfNrDA0nGFBs_PC9Ba_zANUxHjhH3VaQ-E130_provenance.
- NP574313.RA9v71StRKkdfNrDA0nGFBs_PC9Ba_zANUxHjhH3VaQ-E130_assertion wasGeneratedBy ECO_0000203 NP574313.RA9v71StRKkdfNrDA0nGFBs_PC9Ba_zANUxHjhH3VaQ-E130_provenance.