Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP927213.RAJwtxoefgxtlDAWKo-dLj9CsVSd8Kcqd6M1eULeej6ak130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP927213.RAJwtxoefgxtlDAWKo-dLj9CsVSd8Kcqd6M1eULeej6ak130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP927213.RAJwtxoefgxtlDAWKo-dLj9CsVSd8Kcqd6M1eULeej6ak130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP927213.RAJwtxoefgxtlDAWKo-dLj9CsVSd8Kcqd6M1eULeej6ak130_provenance.
- NP927213.RAJwtxoefgxtlDAWKo-dLj9CsVSd8Kcqd6M1eULeej6ak130_assertion description "[We investigated the proteolipid protein (PLP) gene of two boys in a Japanese family with Pelizaeus-Merzbacher disease (PMD), an X-linked neurologic disorder characterized by dysmyelination in the central nervous system (CNS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927213.RAJwtxoefgxtlDAWKo-dLj9CsVSd8Kcqd6M1eULeej6ak130_provenance.
- NP927213.RAJwtxoefgxtlDAWKo-dLj9CsVSd8Kcqd6M1eULeej6ak130_assertion evidence source_evidence_literature NP927213.RAJwtxoefgxtlDAWKo-dLj9CsVSd8Kcqd6M1eULeej6ak130_provenance.
- NP927213.RAJwtxoefgxtlDAWKo-dLj9CsVSd8Kcqd6M1eULeej6ak130_assertion SIO_000772 7683951 NP927213.RAJwtxoefgxtlDAWKo-dLj9CsVSd8Kcqd6M1eULeej6ak130_provenance.
- NP927213.RAJwtxoefgxtlDAWKo-dLj9CsVSd8Kcqd6M1eULeej6ak130_assertion wasDerivedFrom befree-20150227 NP927213.RAJwtxoefgxtlDAWKo-dLj9CsVSd8Kcqd6M1eULeej6ak130_provenance.
- NP927213.RAJwtxoefgxtlDAWKo-dLj9CsVSd8Kcqd6M1eULeej6ak130_assertion wasGeneratedBy ECO_0000203 NP927213.RAJwtxoefgxtlDAWKo-dLj9CsVSd8Kcqd6M1eULeej6ak130_provenance.
- befree-20150227 importedOn "2015-02-27" NP927213.RAJwtxoefgxtlDAWKo-dLj9CsVSd8Kcqd6M1eULeej6ak130_provenance.