Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP584644.RAjd90X9yHV2kYejzVWlWte9oCLgyyHd22Q1w8vjLAWGU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584644.RAjd90X9yHV2kYejzVWlWte9oCLgyyHd22Q1w8vjLAWGU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584644.RAjd90X9yHV2kYejzVWlWte9oCLgyyHd22Q1w8vjLAWGU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584644.RAjd90X9yHV2kYejzVWlWte9oCLgyyHd22Q1w8vjLAWGU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP584644.RAjd90X9yHV2kYejzVWlWte9oCLgyyHd22Q1w8vjLAWGU130_provenance.
- NP584644.RAjd90X9yHV2kYejzVWlWte9oCLgyyHd22Q1w8vjLAWGU130_assertion wasGeneratedBy ECO_0000203 NP584644.RAjd90X9yHV2kYejzVWlWte9oCLgyyHd22Q1w8vjLAWGU130_provenance.
- NP584644.RAjd90X9yHV2kYejzVWlWte9oCLgyyHd22Q1w8vjLAWGU130_assertion wasDerivedFrom befree-20150227 NP584644.RAjd90X9yHV2kYejzVWlWte9oCLgyyHd22Q1w8vjLAWGU130_provenance.
- NP584644.RAjd90X9yHV2kYejzVWlWte9oCLgyyHd22Q1w8vjLAWGU130_assertion SIO_000772 9748047 NP584644.RAjd90X9yHV2kYejzVWlWte9oCLgyyHd22Q1w8vjLAWGU130_provenance.
- NP584644.RAjd90X9yHV2kYejzVWlWte9oCLgyyHd22Q1w8vjLAWGU130_assertion evidence source_evidence_literature NP584644.RAjd90X9yHV2kYejzVWlWte9oCLgyyHd22Q1w8vjLAWGU130_provenance.
- NP584644.RAjd90X9yHV2kYejzVWlWte9oCLgyyHd22Q1w8vjLAWGU130_assertion description "[A Chinese male infant with arthrogryposis multiplex congenita (AMC), ventricular and atrial septal defects, and Werdnig-Hoffmann disease (WHD) had deletions of the telomeric copy of the survival motor neuron (SMN(T)) and neuronal apoptosis inhibitory protein genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584644.RAjd90X9yHV2kYejzVWlWte9oCLgyyHd22Q1w8vjLAWGU130_provenance.