Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP800523.RAAkPUGVD_ASSc5BkVyanB6YhGvXRYP_h03kRpoCI8UDI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP800523.RAAkPUGVD_ASSc5BkVyanB6YhGvXRYP_h03kRpoCI8UDI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800523.RAAkPUGVD_ASSc5BkVyanB6YhGvXRYP_h03kRpoCI8UDI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800523.RAAkPUGVD_ASSc5BkVyanB6YhGvXRYP_h03kRpoCI8UDI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP800523.RAAkPUGVD_ASSc5BkVyanB6YhGvXRYP_h03kRpoCI8UDI130_provenance.
- NP800523.RAAkPUGVD_ASSc5BkVyanB6YhGvXRYP_h03kRpoCI8UDI130_assertion wasGeneratedBy ECO_0000203 NP800523.RAAkPUGVD_ASSc5BkVyanB6YhGvXRYP_h03kRpoCI8UDI130_provenance.
- NP800523.RAAkPUGVD_ASSc5BkVyanB6YhGvXRYP_h03kRpoCI8UDI130_assertion wasDerivedFrom befree-20150227 NP800523.RAAkPUGVD_ASSc5BkVyanB6YhGvXRYP_h03kRpoCI8UDI130_provenance.
- NP800523.RAAkPUGVD_ASSc5BkVyanB6YhGvXRYP_h03kRpoCI8UDI130_assertion SIO_000772 15317749 NP800523.RAAkPUGVD_ASSc5BkVyanB6YhGvXRYP_h03kRpoCI8UDI130_provenance.
- NP800523.RAAkPUGVD_ASSc5BkVyanB6YhGvXRYP_h03kRpoCI8UDI130_assertion evidence source_evidence_literature NP800523.RAAkPUGVD_ASSc5BkVyanB6YhGvXRYP_h03kRpoCI8UDI130_provenance.
- NP800523.RAAkPUGVD_ASSc5BkVyanB6YhGvXRYP_h03kRpoCI8UDI130_assertion description "[Expression of specific genes in liver was analysed, comparing one of these siblings with a child homozygous for missense mutation in ABCB11, as well as with a child having idiopathic cholestatic liver disease, a child with extrahepatic biliary atresia and a normal organ donor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800523.RAAkPUGVD_ASSc5BkVyanB6YhGvXRYP_h03kRpoCI8UDI130_provenance.