Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1017847.RAsBdmGhaiQFVepD1r9kRYg-02it74hzCQx-H7aEJYM5k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1017847.RAsBdmGhaiQFVepD1r9kRYg-02it74hzCQx-H7aEJYM5k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1017847.RAsBdmGhaiQFVepD1r9kRYg-02it74hzCQx-H7aEJYM5k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1017847.RAsBdmGhaiQFVepD1r9kRYg-02it74hzCQx-H7aEJYM5k130_provenance.
- NP1017847.RAsBdmGhaiQFVepD1r9kRYg-02it74hzCQx-H7aEJYM5k130_assertion description "[OFD1, now recognized as a ciliopathy, is characterized by malformations of the face, oral cavity and digits, and is transmitted as an X-linked condition with lethality in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1017847.RAsBdmGhaiQFVepD1r9kRYg-02it74hzCQx-H7aEJYM5k130_provenance.
- NP1017847.RAsBdmGhaiQFVepD1r9kRYg-02it74hzCQx-H7aEJYM5k130_assertion evidence source_evidence_literature NP1017847.RAsBdmGhaiQFVepD1r9kRYg-02it74hzCQx-H7aEJYM5k130_provenance.
- NP1017847.RAsBdmGhaiQFVepD1r9kRYg-02it74hzCQx-H7aEJYM5k130_assertion SIO_000772 23033313 NP1017847.RAsBdmGhaiQFVepD1r9kRYg-02it74hzCQx-H7aEJYM5k130_provenance.
- NP1017847.RAsBdmGhaiQFVepD1r9kRYg-02it74hzCQx-H7aEJYM5k130_assertion wasDerivedFrom befree-2016 NP1017847.RAsBdmGhaiQFVepD1r9kRYg-02it74hzCQx-H7aEJYM5k130_provenance.
- NP1017847.RAsBdmGhaiQFVepD1r9kRYg-02it74hzCQx-H7aEJYM5k130_assertion wasGeneratedBy ECO_0000203 NP1017847.RAsBdmGhaiQFVepD1r9kRYg-02it74hzCQx-H7aEJYM5k130_provenance.
- befree-2016 importedOn "2016-02-19" NP1017847.RAsBdmGhaiQFVepD1r9kRYg-02it74hzCQx-H7aEJYM5k130_provenance.