Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP53218.RApozihwomAxFF6C3SOqcN0rMLkVvCW1nLF9rw6ZtQ_Ps130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP53218.RApozihwomAxFF6C3SOqcN0rMLkVvCW1nLF9rw6ZtQ_Ps130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP53218.RApozihwomAxFF6C3SOqcN0rMLkVvCW1nLF9rw6ZtQ_Ps130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP53218.RApozihwomAxFF6C3SOqcN0rMLkVvCW1nLF9rw6ZtQ_Ps130_provenance.
- NP53218.RApozihwomAxFF6C3SOqcN0rMLkVvCW1nLF9rw6ZtQ_Ps130_assertion description "[We conclude that the F13A1 V34L polymorphism was not associated with the presence of PAD in our study, but may be linked to a later onset of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53218.RApozihwomAxFF6C3SOqcN0rMLkVvCW1nLF9rw6ZtQ_Ps130_provenance.
- NP53218.RApozihwomAxFF6C3SOqcN0rMLkVvCW1nLF9rw6ZtQ_Ps130_assertion evidence source_evidence_literature NP53218.RApozihwomAxFF6C3SOqcN0rMLkVvCW1nLF9rw6ZtQ_Ps130_provenance.
- NP53218.RApozihwomAxFF6C3SOqcN0rMLkVvCW1nLF9rw6ZtQ_Ps130_assertion SIO_000772 11941274 NP53218.RApozihwomAxFF6C3SOqcN0rMLkVvCW1nLF9rw6ZtQ_Ps130_provenance.
- NP53218.RApozihwomAxFF6C3SOqcN0rMLkVvCW1nLF9rw6ZtQ_Ps130_assertion wasDerivedFrom gad-20150221 NP53218.RApozihwomAxFF6C3SOqcN0rMLkVvCW1nLF9rw6ZtQ_Ps130_provenance.
- NP53218.RApozihwomAxFF6C3SOqcN0rMLkVvCW1nLF9rw6ZtQ_Ps130_assertion wasGeneratedBy ECO_0000203 NP53218.RApozihwomAxFF6C3SOqcN0rMLkVvCW1nLF9rw6ZtQ_Ps130_provenance.
- gad-20150221 importedOn "2015-02-21" NP53218.RApozihwomAxFF6C3SOqcN0rMLkVvCW1nLF9rw6ZtQ_Ps130_provenance.