Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP690001.RAgczVUInV9Q1lchVu4m20jnQ15Sto1Pi0COm66g8WnsU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP690001.RAgczVUInV9Q1lchVu4m20jnQ15Sto1Pi0COm66g8WnsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690001.RAgczVUInV9Q1lchVu4m20jnQ15Sto1Pi0COm66g8WnsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690001.RAgczVUInV9Q1lchVu4m20jnQ15Sto1Pi0COm66g8WnsU130_provenance.
- NP690001.RAgczVUInV9Q1lchVu4m20jnQ15Sto1Pi0COm66g8WnsU130_assertion description "[Several studies have attempted to demonstrate the association of the most intensively examined variant of P-selectin gene polymorphism (Thr715Pro) with sP-selectin levels in healthy subjects and in CVD, but contradictory data have been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690001.RAgczVUInV9Q1lchVu4m20jnQ15Sto1Pi0COm66g8WnsU130_provenance.
- NP690001.RAgczVUInV9Q1lchVu4m20jnQ15Sto1Pi0COm66g8WnsU130_assertion evidence source_evidence_literature NP690001.RAgczVUInV9Q1lchVu4m20jnQ15Sto1Pi0COm66g8WnsU130_provenance.
- NP690001.RAgczVUInV9Q1lchVu4m20jnQ15Sto1Pi0COm66g8WnsU130_assertion SIO_000772 17598012 NP690001.RAgczVUInV9Q1lchVu4m20jnQ15Sto1Pi0COm66g8WnsU130_provenance.
- NP690001.RAgczVUInV9Q1lchVu4m20jnQ15Sto1Pi0COm66g8WnsU130_assertion wasDerivedFrom befree-20150227 NP690001.RAgczVUInV9Q1lchVu4m20jnQ15Sto1Pi0COm66g8WnsU130_provenance.
- NP690001.RAgczVUInV9Q1lchVu4m20jnQ15Sto1Pi0COm66g8WnsU130_assertion wasGeneratedBy ECO_0000203 NP690001.RAgczVUInV9Q1lchVu4m20jnQ15Sto1Pi0COm66g8WnsU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP690001.RAgczVUInV9Q1lchVu4m20jnQ15Sto1Pi0COm66g8WnsU130_provenance.