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- source_evidence_literature type ECO_0000212 NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_provenance.
- NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_assertion wasGeneratedBy ECO_0000203 NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_provenance.
- NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_assertion wasDerivedFrom befree-20150227 NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_provenance.
- NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_assertion SIO_000772 21236492 NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_provenance.
- NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_assertion evidence source_evidence_literature NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_provenance.
- NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_assertion description "[A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_provenance.