Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_assertion> ?p ?o ?g. }
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- NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_assertion type Assertion NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_head.
- 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.