Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1327141.RAA-IKFjIHSFwBGtlBRk8_LoexPAEKRJoN5zR4BVLu1TU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1327141.RAA-IKFjIHSFwBGtlBRk8_LoexPAEKRJoN5zR4BVLu1TU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1327141.RAA-IKFjIHSFwBGtlBRk8_LoexPAEKRJoN5zR4BVLu1TU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1327141.RAA-IKFjIHSFwBGtlBRk8_LoexPAEKRJoN5zR4BVLu1TU130_provenance.
- NP1327141.RAA-IKFjIHSFwBGtlBRk8_LoexPAEKRJoN5zR4BVLu1TU130_assertion description "[The rare apolipoprotein C-II (apoC-II) mutation, apoC-IILys19-->Thr, also known as apoC-II-v, has been found previously in association with hyperlipoproteinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327141.RAA-IKFjIHSFwBGtlBRk8_LoexPAEKRJoN5zR4BVLu1TU130_provenance.
- NP1327141.RAA-IKFjIHSFwBGtlBRk8_LoexPAEKRJoN5zR4BVLu1TU130_assertion evidence source_evidence_literature NP1327141.RAA-IKFjIHSFwBGtlBRk8_LoexPAEKRJoN5zR4BVLu1TU130_provenance.
- NP1327141.RAA-IKFjIHSFwBGtlBRk8_LoexPAEKRJoN5zR4BVLu1TU130_assertion SIO_000772 7923858 NP1327141.RAA-IKFjIHSFwBGtlBRk8_LoexPAEKRJoN5zR4BVLu1TU130_provenance.
- NP1327141.RAA-IKFjIHSFwBGtlBRk8_LoexPAEKRJoN5zR4BVLu1TU130_assertion wasDerivedFrom befree-2016 NP1327141.RAA-IKFjIHSFwBGtlBRk8_LoexPAEKRJoN5zR4BVLu1TU130_provenance.
- NP1327141.RAA-IKFjIHSFwBGtlBRk8_LoexPAEKRJoN5zR4BVLu1TU130_assertion wasGeneratedBy ECO_0000203 NP1327141.RAA-IKFjIHSFwBGtlBRk8_LoexPAEKRJoN5zR4BVLu1TU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1327141.RAA-IKFjIHSFwBGtlBRk8_LoexPAEKRJoN5zR4BVLu1TU130_provenance.