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- source_evidence_literature type ECO_0000212 NP256110.RAON8vocvU7Jgs2JjBO7ELWaWH488EdltsXURsdekttFo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256110.RAON8vocvU7Jgs2JjBO7ELWaWH488EdltsXURsdekttFo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256110.RAON8vocvU7Jgs2JjBO7ELWaWH488EdltsXURsdekttFo130_provenance.
- NP256110.RAON8vocvU7Jgs2JjBO7ELWaWH488EdltsXURsdekttFo130_assertion description "[Many novel ATP1A2 mutations were identified in patients with familial and sporadic hemiplegic migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256110.RAON8vocvU7Jgs2JjBO7ELWaWH488EdltsXURsdekttFo130_provenance.
- NP256110.RAON8vocvU7Jgs2JjBO7ELWaWH488EdltsXURsdekttFo130_assertion evidence source_evidence_literature NP256110.RAON8vocvU7Jgs2JjBO7ELWaWH488EdltsXURsdekttFo130_provenance.
- NP256110.RAON8vocvU7Jgs2JjBO7ELWaWH488EdltsXURsdekttFo130_assertion SIO_000772 18451712 NP256110.RAON8vocvU7Jgs2JjBO7ELWaWH488EdltsXURsdekttFo130_provenance.
- NP256110.RAON8vocvU7Jgs2JjBO7ELWaWH488EdltsXURsdekttFo130_assertion wasDerivedFrom befree-20150227 NP256110.RAON8vocvU7Jgs2JjBO7ELWaWH488EdltsXURsdekttFo130_provenance.
- NP256110.RAON8vocvU7Jgs2JjBO7ELWaWH488EdltsXURsdekttFo130_assertion wasGeneratedBy ECO_0000203 NP256110.RAON8vocvU7Jgs2JjBO7ELWaWH488EdltsXURsdekttFo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP256110.RAON8vocvU7Jgs2JjBO7ELWaWH488EdltsXURsdekttFo130_provenance.