Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP591066.RAF4NCZl19gr6IuGsi_I4Xym6EXC8Mre8AOXdhSAvJL0Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP591066.RAF4NCZl19gr6IuGsi_I4Xym6EXC8Mre8AOXdhSAvJL0Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP591066.RAF4NCZl19gr6IuGsi_I4Xym6EXC8Mre8AOXdhSAvJL0Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP591066.RAF4NCZl19gr6IuGsi_I4Xym6EXC8Mre8AOXdhSAvJL0Y130_provenance.
- NP591066.RAF4NCZl19gr6IuGsi_I4Xym6EXC8Mre8AOXdhSAvJL0Y130_assertion description "[Subsequent studies revealed that the great majority of afibrinogenemia mutations are localized in FGA, but mutations were also found in FGG and FGB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591066.RAF4NCZl19gr6IuGsi_I4Xym6EXC8Mre8AOXdhSAvJL0Y130_provenance.
- NP591066.RAF4NCZl19gr6IuGsi_I4Xym6EXC8Mre8AOXdhSAvJL0Y130_assertion evidence source_evidence_literature NP591066.RAF4NCZl19gr6IuGsi_I4Xym6EXC8Mre8AOXdhSAvJL0Y130_provenance.
- NP591066.RAF4NCZl19gr6IuGsi_I4Xym6EXC8Mre8AOXdhSAvJL0Y130_assertion SIO_000772 12893758 NP591066.RAF4NCZl19gr6IuGsi_I4Xym6EXC8Mre8AOXdhSAvJL0Y130_provenance.
- NP591066.RAF4NCZl19gr6IuGsi_I4Xym6EXC8Mre8AOXdhSAvJL0Y130_assertion wasDerivedFrom befree-20140225 NP591066.RAF4NCZl19gr6IuGsi_I4Xym6EXC8Mre8AOXdhSAvJL0Y130_provenance.
- NP591066.RAF4NCZl19gr6IuGsi_I4Xym6EXC8Mre8AOXdhSAvJL0Y130_assertion wasGeneratedBy ECO_0000203 NP591066.RAF4NCZl19gr6IuGsi_I4Xym6EXC8Mre8AOXdhSAvJL0Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP591066.RAF4NCZl19gr6IuGsi_I4Xym6EXC8Mre8AOXdhSAvJL0Y130_provenance.