Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP324304.RAlUhAQ8PNw6FLLSgmqUEfQeNo81wkx3GDtSMCUVPVQi4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP324304.RAlUhAQ8PNw6FLLSgmqUEfQeNo81wkx3GDtSMCUVPVQi4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP324304.RAlUhAQ8PNw6FLLSgmqUEfQeNo81wkx3GDtSMCUVPVQi4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP324304.RAlUhAQ8PNw6FLLSgmqUEfQeNo81wkx3GDtSMCUVPVQi4130_provenance.
- NP324304.RAlUhAQ8PNw6FLLSgmqUEfQeNo81wkx3GDtSMCUVPVQi4130_assertion description "[Homozygous VN (677C to T) and d/D (2756G to A) variants in the methylenetetrahydrofolate and methionine synthase genes in a case of hyperhomocysteinemia with stroke at young age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324304.RAlUhAQ8PNw6FLLSgmqUEfQeNo81wkx3GDtSMCUVPVQi4130_provenance.
- NP324304.RAlUhAQ8PNw6FLLSgmqUEfQeNo81wkx3GDtSMCUVPVQi4130_assertion evidence source_evidence_literature NP324304.RAlUhAQ8PNw6FLLSgmqUEfQeNo81wkx3GDtSMCUVPVQi4130_provenance.
- NP324304.RAlUhAQ8PNw6FLLSgmqUEfQeNo81wkx3GDtSMCUVPVQi4130_assertion SIO_000772 11460881 NP324304.RAlUhAQ8PNw6FLLSgmqUEfQeNo81wkx3GDtSMCUVPVQi4130_provenance.
- NP324304.RAlUhAQ8PNw6FLLSgmqUEfQeNo81wkx3GDtSMCUVPVQi4130_assertion wasDerivedFrom befree-2016 NP324304.RAlUhAQ8PNw6FLLSgmqUEfQeNo81wkx3GDtSMCUVPVQi4130_provenance.
- NP324304.RAlUhAQ8PNw6FLLSgmqUEfQeNo81wkx3GDtSMCUVPVQi4130_assertion wasGeneratedBy ECO_0000203 NP324304.RAlUhAQ8PNw6FLLSgmqUEfQeNo81wkx3GDtSMCUVPVQi4130_provenance.
- befree-2016 importedOn "2016-02-19" NP324304.RAlUhAQ8PNw6FLLSgmqUEfQeNo81wkx3GDtSMCUVPVQi4130_provenance.