Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP432722.RA3jC_H7s5Zru_V9AWncga4RQHpcoQnEeBxvWKdouaRBY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP432722.RA3jC_H7s5Zru_V9AWncga4RQHpcoQnEeBxvWKdouaRBY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP432722.RA3jC_H7s5Zru_V9AWncga4RQHpcoQnEeBxvWKdouaRBY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP432722.RA3jC_H7s5Zru_V9AWncga4RQHpcoQnEeBxvWKdouaRBY130_provenance.
- NP432722.RA3jC_H7s5Zru_V9AWncga4RQHpcoQnEeBxvWKdouaRBY130_assertion description "[In other families with dominant HEPACAM mutations, patients had macrocephaly and mental retardation with or without autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP432722.RA3jC_H7s5Zru_V9AWncga4RQHpcoQnEeBxvWKdouaRBY130_provenance.
- NP432722.RA3jC_H7s5Zru_V9AWncga4RQHpcoQnEeBxvWKdouaRBY130_assertion evidence source_evidence_literature NP432722.RA3jC_H7s5Zru_V9AWncga4RQHpcoQnEeBxvWKdouaRBY130_provenance.
- NP432722.RA3jC_H7s5Zru_V9AWncga4RQHpcoQnEeBxvWKdouaRBY130_assertion SIO_000772 21419380 NP432722.RA3jC_H7s5Zru_V9AWncga4RQHpcoQnEeBxvWKdouaRBY130_provenance.
- NP432722.RA3jC_H7s5Zru_V9AWncga4RQHpcoQnEeBxvWKdouaRBY130_assertion wasDerivedFrom befree-20140225 NP432722.RA3jC_H7s5Zru_V9AWncga4RQHpcoQnEeBxvWKdouaRBY130_provenance.
- NP432722.RA3jC_H7s5Zru_V9AWncga4RQHpcoQnEeBxvWKdouaRBY130_assertion wasGeneratedBy ECO_0000203 NP432722.RA3jC_H7s5Zru_V9AWncga4RQHpcoQnEeBxvWKdouaRBY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP432722.RA3jC_H7s5Zru_V9AWncga4RQHpcoQnEeBxvWKdouaRBY130_provenance.