Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP719867.RAd8IQCx6Eh8HbUJqND4j78fNeCgCu6-7aS2m4GjQuF2k130_assertion> ?p ?o ?g. }
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- NP719867.RAd8IQCx6Eh8HbUJqND4j78fNeCgCu6-7aS2m4GjQuF2k130_assertion type Assertion NP719867.RAd8IQCx6Eh8HbUJqND4j78fNeCgCu6-7aS2m4GjQuF2k130_head.
- NP719867.RAd8IQCx6Eh8HbUJqND4j78fNeCgCu6-7aS2m4GjQuF2k130_assertion description "[Mutations in the NBS1 gene are responsible for Nijmegen breakage syndrome (NBS), a hereditary disorder that imparts an increased predisposition to development of malignancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719867.RAd8IQCx6Eh8HbUJqND4j78fNeCgCu6-7aS2m4GjQuF2k130_provenance.
- NP719867.RAd8IQCx6Eh8HbUJqND4j78fNeCgCu6-7aS2m4GjQuF2k130_assertion evidence source_evidence_literature NP719867.RAd8IQCx6Eh8HbUJqND4j78fNeCgCu6-7aS2m4GjQuF2k130_provenance.
- NP719867.RAd8IQCx6Eh8HbUJqND4j78fNeCgCu6-7aS2m4GjQuF2k130_assertion SIO_000772 16467875 NP719867.RAd8IQCx6Eh8HbUJqND4j78fNeCgCu6-7aS2m4GjQuF2k130_provenance.
- NP719867.RAd8IQCx6Eh8HbUJqND4j78fNeCgCu6-7aS2m4GjQuF2k130_assertion wasDerivedFrom befree-20140225 NP719867.RAd8IQCx6Eh8HbUJqND4j78fNeCgCu6-7aS2m4GjQuF2k130_provenance.
- NP719867.RAd8IQCx6Eh8HbUJqND4j78fNeCgCu6-7aS2m4GjQuF2k130_assertion wasGeneratedBy ECO_0000203 NP719867.RAd8IQCx6Eh8HbUJqND4j78fNeCgCu6-7aS2m4GjQuF2k130_provenance.