Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP626413.RAHOnWPhmHopB_4yWc1pLR8yG5NwRy36Uj37thOpV66CU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP626413.RAHOnWPhmHopB_4yWc1pLR8yG5NwRy36Uj37thOpV66CU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626413.RAHOnWPhmHopB_4yWc1pLR8yG5NwRy36Uj37thOpV66CU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626413.RAHOnWPhmHopB_4yWc1pLR8yG5NwRy36Uj37thOpV66CU130_provenance.
- NP626413.RAHOnWPhmHopB_4yWc1pLR8yG5NwRy36Uj37thOpV66CU130_assertion description "[Cytogenetically invisible microdeletions involving PITX2 in Rieger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626413.RAHOnWPhmHopB_4yWc1pLR8yG5NwRy36Uj37thOpV66CU130_provenance.
- NP626413.RAHOnWPhmHopB_4yWc1pLR8yG5NwRy36Uj37thOpV66CU130_assertion evidence source_evidence_literature NP626413.RAHOnWPhmHopB_4yWc1pLR8yG5NwRy36Uj37thOpV66CU130_provenance.
- NP626413.RAHOnWPhmHopB_4yWc1pLR8yG5NwRy36Uj37thOpV66CU130_assertion SIO_000772 17850355 NP626413.RAHOnWPhmHopB_4yWc1pLR8yG5NwRy36Uj37thOpV66CU130_provenance.
- NP626413.RAHOnWPhmHopB_4yWc1pLR8yG5NwRy36Uj37thOpV66CU130_assertion wasDerivedFrom befree-20150227 NP626413.RAHOnWPhmHopB_4yWc1pLR8yG5NwRy36Uj37thOpV66CU130_provenance.
- NP626413.RAHOnWPhmHopB_4yWc1pLR8yG5NwRy36Uj37thOpV66CU130_assertion wasGeneratedBy ECO_0000203 NP626413.RAHOnWPhmHopB_4yWc1pLR8yG5NwRy36Uj37thOpV66CU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP626413.RAHOnWPhmHopB_4yWc1pLR8yG5NwRy36Uj37thOpV66CU130_provenance.