Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977257.RA4H2PvyrcRcA_fXY6srpCUHNCyMgVe_u2Gwu2ZQrtlF0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP977257.RA4H2PvyrcRcA_fXY6srpCUHNCyMgVe_u2Gwu2ZQrtlF0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977257.RA4H2PvyrcRcA_fXY6srpCUHNCyMgVe_u2Gwu2ZQrtlF0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977257.RA4H2PvyrcRcA_fXY6srpCUHNCyMgVe_u2Gwu2ZQrtlF0130_provenance.
- NP977257.RA4H2PvyrcRcA_fXY6srpCUHNCyMgVe_u2Gwu2ZQrtlF0130_assertion description "[The novel findings included a set of genes (DCDC2, DYX1C1, KIAA0319) related to a neurological disease dyslexia suggesting their potential involvement in ciliary functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977257.RA4H2PvyrcRcA_fXY6srpCUHNCyMgVe_u2Gwu2ZQrtlF0130_provenance.
- NP977257.RA4H2PvyrcRcA_fXY6srpCUHNCyMgVe_u2Gwu2ZQrtlF0130_assertion evidence source_evidence_literature NP977257.RA4H2PvyrcRcA_fXY6srpCUHNCyMgVe_u2Gwu2ZQrtlF0130_provenance.
- NP977257.RA4H2PvyrcRcA_fXY6srpCUHNCyMgVe_u2Gwu2ZQrtlF0130_assertion SIO_000772 22558177 NP977257.RA4H2PvyrcRcA_fXY6srpCUHNCyMgVe_u2Gwu2ZQrtlF0130_provenance.
- NP977257.RA4H2PvyrcRcA_fXY6srpCUHNCyMgVe_u2Gwu2ZQrtlF0130_assertion wasDerivedFrom befree-20150227 NP977257.RA4H2PvyrcRcA_fXY6srpCUHNCyMgVe_u2Gwu2ZQrtlF0130_provenance.
- NP977257.RA4H2PvyrcRcA_fXY6srpCUHNCyMgVe_u2Gwu2ZQrtlF0130_assertion wasGeneratedBy ECO_0000203 NP977257.RA4H2PvyrcRcA_fXY6srpCUHNCyMgVe_u2Gwu2ZQrtlF0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977257.RA4H2PvyrcRcA_fXY6srpCUHNCyMgVe_u2Gwu2ZQrtlF0130_provenance.