Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925672.RAYG8VnM3vKJzQv4RL6MXpmGtoVQxk8wu_z_KrRCV2Zp0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925672.RAYG8VnM3vKJzQv4RL6MXpmGtoVQxk8wu_z_KrRCV2Zp0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925672.RAYG8VnM3vKJzQv4RL6MXpmGtoVQxk8wu_z_KrRCV2Zp0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925672.RAYG8VnM3vKJzQv4RL6MXpmGtoVQxk8wu_z_KrRCV2Zp0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP925672.RAYG8VnM3vKJzQv4RL6MXpmGtoVQxk8wu_z_KrRCV2Zp0130_provenance.
- NP925672.RAYG8VnM3vKJzQv4RL6MXpmGtoVQxk8wu_z_KrRCV2Zp0130_assertion wasGeneratedBy ECO_0000203 NP925672.RAYG8VnM3vKJzQv4RL6MXpmGtoVQxk8wu_z_KrRCV2Zp0130_provenance.
- NP925672.RAYG8VnM3vKJzQv4RL6MXpmGtoVQxk8wu_z_KrRCV2Zp0130_assertion wasDerivedFrom befree-20150227 NP925672.RAYG8VnM3vKJzQv4RL6MXpmGtoVQxk8wu_z_KrRCV2Zp0130_provenance.
- NP925672.RAYG8VnM3vKJzQv4RL6MXpmGtoVQxk8wu_z_KrRCV2Zp0130_assertion SIO_000772 2148653 NP925672.RAYG8VnM3vKJzQv4RL6MXpmGtoVQxk8wu_z_KrRCV2Zp0130_provenance.
- NP925672.RAYG8VnM3vKJzQv4RL6MXpmGtoVQxk8wu_z_KrRCV2Zp0130_assertion evidence source_evidence_literature NP925672.RAYG8VnM3vKJzQv4RL6MXpmGtoVQxk8wu_z_KrRCV2Zp0130_provenance.
- NP925672.RAYG8VnM3vKJzQv4RL6MXpmGtoVQxk8wu_z_KrRCV2Zp0130_assertion description "[In a group of 37 consecutive patients with arterial occlusive disease presenting before the age of 45, three patients were found heterozygous for hereditary protein S deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925672.RAYG8VnM3vKJzQv4RL6MXpmGtoVQxk8wu_z_KrRCV2Zp0130_provenance.