Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_provenance.
- NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_assertion description "[Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_provenance.
- NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_assertion evidence source_evidence_literature NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_provenance.
- NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_assertion SIO_000772 23768516 NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_provenance.
- NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_assertion wasDerivedFrom befree-20150227 NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_provenance.
- NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_assertion wasGeneratedBy ECO_0000203 NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_provenance.